CRYBG1
crystallin beta-gamma domain containing 1
Summary
Predicted to enable carbohydrate binding activity. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants117 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6568433 | 6:106,829,537 | T/G | — | — |
| rs111829969 | 6:106,863,768 | C/T | — | — |
| rs542468253 | 6:106,866,895 | G/A | — | — |
| rs1417352 | 6:106,899,226 | C/T | upstream gene variant | — |
| rs752323326 | 6:106,960,263 | C/T | — | uncertain significance |
| rs753454001 | 6:106,960,277 | G/C | — | uncertain significance |
| rs201789082 | 6:106,960,382 | G/C | — | uncertain significance |
| rs1398695376 | 6:106,960,388 | A/G | — | uncertain significance |
| rs758138078 | 6:106,960,436 | G/T | — | uncertain significance |
| rs11152999 | 6:106,960,447 | G/A | synonymous variant | — |
| rs1175910374 | 6:106,960,467 | C/A | — | uncertain significance |
| rs748683370 | 6:106,960,595 | G/T | — | uncertain significance |
| rs1399326782 | 6:106,960,607 | G/A | — | uncertain significance |
| rs767378767 | 6:106,960,659 | C/T | — | uncertain significance |
| rs773473919 | 6:106,960,700 | G/A | — | uncertain significance |
| rs946413097 | 6:106,960,707 | C/T | — | uncertain significance |
| rs746845033 | 6:106,960,799 | C/G | — | uncertain significance |
| rs766309134 | 6:106,960,820 | G/A | — | uncertain significance |
| rs774273556 | 6:106,960,871 | C/A | — | uncertain significance |
| rs140867686 | 6:106,967,146 | G/A | — | uncertain significance |
| rs368643208 | 6:106,967,167 | A/G | — | uncertain significance |
| rs201575286 | 6:106,967,212 | C/T | — | uncertain significance |
| rs761551205 | 6:106,967,226 | G/A | — | uncertain significance |
| rs761415263 | 6:106,967,350 | C/T | — | uncertain significance |
| rs2482090943 | 6:106,967,512 | A/G | — | uncertain significance |
| rs140934013 | 6:106,967,565 | C/T | — | uncertain significance |
| rs377596539 | 6:106,967,632 | C/G | — | uncertain significance |
| rs777401307 | 6:106,967,635 | C/T | — | uncertain significance |
| rs941622898 | 6:106,967,719 | C/A | — | uncertain significance |
| rs144881884 | 6:106,967,831 | T/C | — | likely benign |
| rs144737726 | 6:106,967,832 | C/T | — | uncertain significance |
| rs746060532 | 6:106,967,852 | G/A | — | uncertain significance |
| rs2482092763 | 6:106,967,854 | C/T | — | uncertain significance |
| rs149735097 | 6:106,967,928 | T/G | — | uncertain significance |
| rs373693413 | 6:106,967,930 | T/G | — | uncertain significance |
| rs181129946 | 6:106,967,946 | G/A | — | uncertain significance |
| rs768609929 | 6:106,967,962 | T/G | — | uncertain significance |
| rs891264418 | 6:106,967,970 | C/T | — | uncertain significance |
| rs765990707 | 6:106,967,991 | G/A | — | uncertain significance |
| rs377195581 | 6:106,968,007 | T/A | — | uncertain significance |
| rs752485338 | 6:106,968,009 | C/T | — | likely benign |
| rs2482094140 | 6:106,968,065 | T/G | — | likely benign |
| rs763893451 | 6:106,968,093 | C/T | — | uncertain significance |
| rs770226107 | 6:106,968,103 | A/T | — | uncertain significance |
| rs2482094975 | 6:106,968,204 | C/G | — | uncertain significance |
| rs746629299 | 6:106,968,252 | C/T | — | uncertain significance |
| rs768343143 | 6:106,968,253 | C/T | — | uncertain significance |
| rs139061896 | 6:106,968,256 | C/A | — | uncertain significance |
| rs201201445 | 6:106,968,273 | G/A | — | likely benign |
| rs371008588 | 6:106,968,288 | A/G | — | uncertain significance |
| rs1176048958 | 6:106,968,398 | G/A | — | uncertain significance |
| rs141256151 | 6:106,968,433 | G/A | — | uncertain significance |
| rs150778380 | 6:106,968,435 | G/A | — | likely benign |
| rs113287212 | 6:106,968,444 | A/G | — | likely benign |
| rs754425255 | 6:106,968,448 | C/T | — | uncertain significance |
| rs751433495 | 6:106,968,465 | G/A | — | uncertain significance |
| rs199579020 | 6:106,968,486 | G/A | — | uncertain significance |
| rs752201884 | 6:106,968,577 | A/G | — | uncertain significance |
| rs61739383 | 6:106,968,671 | G/A | — | likely benign |
| rs2482097248 | 6:106,968,679 | T/C | — | uncertain significance |
| rs1409828910 | 6:106,968,726 | G/C | — | uncertain significance |
| rs199754054 | 6:106,968,747 | A/G | — | uncertain significance |
| rs777887660 | 6:106,968,765 | A/T | — | uncertain significance |
| rs777312523 | 6:106,968,820 | T/G | — | uncertain significance |
| rs200028219 | 6:106,968,850 | T/C | — | uncertain significance |
| rs2482098309 | 6:106,968,864 | A/G | — | uncertain significance |
| rs769073910 | 6:106,968,913 | C/T | — | uncertain significance |
| rs1309816516 | 6:106,969,036 | G/T | — | uncertain significance |
| rs1008705878 | 6:106,969,045 | A/G | — | uncertain significance |
| rs150414602 | 6:106,969,085 | G/A | — | likely benign |
| rs533984443 | 6:106,969,120 | G/A | — | uncertain significance |
| rs2482099790 | 6:106,969,143 | A/G | — | uncertain significance |
| rs759942742 | 6:106,969,318 | C/T | — | uncertain significance |
| rs770941687 | 6:106,973,047 | C/G | — | uncertain significance |
| rs151152423 | 6:106,973,164 | G/A | — | uncertain significance |
| rs184010756 | 6:106,973,234 | T/A | — | uncertain significance |
| rs751496015 | 6:106,975,304 | G/A | — | uncertain significance |
| rs2482126103 | 6:106,978,134 | A/C | — | uncertain significance |
| rs760703728 | 6:106,978,182 | T/G | — | uncertain significance |
| rs783396 | 6:106,987,370 | A/G | missense variant | — |
| rs2482150337 | 6:106,987,373 | C/T | — | uncertain significance |
| rs1315196622 | 6:106,991,366 | A/T | — | uncertain significance |
| rs200123421 | 6:106,991,367 | C/T | — | uncertain significance |
| rs146009064 | 6:106,991,409 | A/G | — | uncertain significance |
| rs572684440 | 6:106,991,412 | C/T | — | uncertain significance |
| rs147230945 | 6:106,991,468 | G/A | — | uncertain significance |
| rs373066793 | 6:106,992,475 | C/T | — | uncertain significance |
| rs1204572922 | 6:106,992,523 | C/G | — | uncertain significance |
| rs144800958 | 6:106,992,539 | T/A | — | uncertain significance |
| rs147938718 | 6:106,992,547 | T/C | — | uncertain significance |
| rs150066642 | 6:106,992,564 | A/G | — | uncertain significance |
| rs369036571 | 6:106,992,733 | T/G | — | uncertain significance |
| rs371775265 | 6:106,992,747 | G/A | — | uncertain significance |
| rs1291253403 | 6:106,992,789 | A/G | — | uncertain significance |
| rs1774413106 | 6:106,999,789 | A/G | — | uncertain significance |
| rs772247383 | 6:107,000,063 | C/T | — | uncertain significance |
| rs2114587374 | 6:107,001,366 | A/T | — | uncertain significance |
| rs745354447 | 6:107,003,672 | C/G | — | likely benign |
| rs1332633973 | 6:107,003,749 | A/C | — | uncertain significance |
| rs779661246 | 6:107,003,758 | C/T | — | uncertain significance |
Showing 100 of 117 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.