LRRC37A
leucine rich repeat containing 37A
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants127 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2668639 | 17:44,324,539 | T/C | downstream gene variant | — |
| rs2696618 | 17:44,325,635 | C/T | — | — |
| rs56368550 | 17:44,326,712 | T/C | downstream gene variant | — |
| rs2696625 | 17:44,326,864 | A/G | — | — |
| rs2696626 | 17:44,327,070 | G/A | downstream gene variant | — |
| rs2458185 | 17:44,327,370 | C/A | downstream gene variant | — |
| rs2696630 | 17:44,327,482 | G/A | intergenic variant | — |
| rs2907480 | 17:44,327,712 | C/A | — | — |
| rs374470873 | 17:44,328,919 | T/C | — | — |
| rs79641193 | 17:44,330,105 | A/G | regulatory region variant | — |
| rs2957316 | 17:44,331,214 | T/C | regulatory region variant | — |
| rs2950015 | 17:44,332,351 | A/G | downstream gene variant | — |
| rs71375338 | 17:44,332,793 | G/A | downstream gene variant | — |
| rs12953096 | 17:44,332,959 | C/T | downstream gene variant | — |
| rs2532363 | 17:44,333,423 | G/T | downstream gene variant | — |
| rs2696422 | 17:44,333,889 | T/C | downstream gene variant | — |
| rs2696423 | 17:44,333,890 | G/A | downstream gene variant | — |
| rs41490145 | 17:44,334,288 | C/G | downstream gene variant | — |
| rs2458179 | 17:44,334,707 | G/C | — | — |
| rs139077859 | 17:44,335,579 | G/A | downstream gene variant | — |
| rs147431626 | 17:44,335,635 | G/A | downstream gene variant | — |
| rs62074563 | 17:44,335,806 | A/G | — | — |
| rs2532353 | 17:44,335,867 | G/T | — | — |
| rs2458203 | 17:44,336,651 | T/A | — | — |
| rs2532351 | 17:44,336,997 | C/A | coding sequence variant | — |
| rs62074568 | 17:44,337,512 | A/T | coding sequence variant | — |
| rs35031964 | 17:44,337,760 | A/G | coding sequence variant | — |
| rs2732689 | 17:44,338,503 | C/A | upstream gene variant | — |
| rs2463514 | 17:44,338,869 | C/T | — | — |
| rs34677756 | 17:44,339,003 | G/T | upstream gene variant | — |
| rs2732685 | 17:44,339,408 | C/T | upstream gene variant | — |
| rs2532349 | 17:44,339,473 | A/G | upstream gene variant | — |
| rs77917260 | 17:44,339,607 | C/T | upstream gene variant | — |
| rs2266456 | 17:44,340,506 | C/T | — | — |
| rs4988900 | 17:44,342,378 | G/C | — | — |
| rs555179559 | 17:44,342,752 | C/T | — | — |
| rs2668716 | 17:44,343,371 | G/A | regulatory region variant | — |
| rs2696692 | 17:44,343,719 | C/T | regulatory region variant | — |
| rs2532344 | 17:44,343,930 | A/G | regulatory region variant | — |
| rs2732650 | 17:44,344,988 | C/T | — | — |
| rs2696557 | 17:44,347,218 | C/A | downstream gene variant | — |
| rs2732712 | 17:44,348,932 | T/C | — | — |
| rs2696546 | 17:44,350,919 | A/C | downstream gene variant | — |
| rs2732708 | 17:44,351,387 | C/T | downstream gene variant | — |
| rs2696542 | 17:44,351,533 | A/G | downstream gene variant | — |
| rs2732706 | 17:44,351,686 | C/T | downstream gene variant | — |
| rs2732703 | 17:44,353,222 | T/G | intron variant | — |
| rs36050210 | 17:44,353,414 | A/C | — | — |
| rs2732702 | 17:44,353,728 | T/G | intron variant | — |
| rs2261201 | 17:44,354,549 | C/G | regulatory region variant | — |
| rs2732699 | 17:44,354,904 | T/G | — | — |
| rs371894855 | 17:44,355,304 | G/T | — | — |
| rs2696532 | 17:44,355,602 | A/G | intron variant | — |
| rs2696531 | 17:44,355,634 | C/G | — | — |
| rs113986870 | 17:44,355,683 | G/A | intron variant | — |
| rs17665188 | 17:44,357,351 | T/C | regulatory region variant | — |
| rs75067210 | 17:44,357,654 | C/T | — | — |
| rs2696518 | 17:44,357,885 | T/G | intron variant | — |
| rs567642046 | 17:44,358,811 | G/A | — | — |
| rs184837332 | 17:44,359,783 | G/T | — | — |
| rs2732620 | 17:44,362,865 | A/T | — | — |
| rs7225145 | 17:44,363,740 | C/A | intron variant | — |
| rs2696500 | 17:44,363,929 | C/T | regulatory region variant | — |
| rs578102530 | 17:44,364,335 | G/T | — | — |
| rs2696499 | 17:44,364,519 | C/G | regulatory region variant | — |
| rs2696497 | 17:44,364,649 | C/T | regulatory region variant | — |
| rs2732610 | 17:44,365,490 | C/T | — | — |
| rs2668654 | 17:44,366,315 | T/C | upstream gene variant | — |
| rs2732600 | 17:44,368,215 | C/A | — | — |
| rs2532424 | 17:44,368,926 | C/A | regulatory region variant | — |
| rs567949023 | 17:44,372,673 | G/C | — | uncertain significance |
| rs2544511972 | 17:44,374,612 | A/G | — | uncertain significance |
| rs1314295373 | 17:44,374,657 | C/T | — | uncertain significance |
| rs1216520046 | 17:44,374,688 | A/T | — | uncertain significance |
| rs62073222 | 17:44,374,710 | A/G | — | benign |
| rs2050196527 | 17:44,374,798 | A/G | — | uncertain significance |
| rs200117012 | 17:44,374,819 | G/A | — | uncertain significance |
| rs1367405331 | 17:44,374,822 | C/T | — | uncertain significance |
| rs1275205266 | 17:44,374,834 | C/T | — | uncertain significance |
| rs557815137 | 17:44,374,837 | G/C | — | likely benign |
| rs1427125348 | 17:44,374,859 | T/C | — | uncertain significance |
| rs1390964754 | 17:44,374,886 | A/T | — | uncertain significance |
| rs2544515323 | 17:44,374,895 | C/G | — | uncertain significance |
| rs1219476453 | 17:44,374,897 | G/A | — | likely benign |
| rs1170408266 | 17:44,374,970 | C/T | — | uncertain significance |
| rs1420156961 | 17:44,374,979 | G/A | — | likely benign |
| rs1441152025 | 17:44,375,071 | C/T | — | likely benign |
| rs1360693040 | 17:44,382,892 | A/T | — | uncertain significance |
| rs1017773862 | 17:44,382,924 | C/T | — | likely benign |
| rs62073233 | 17:44,388,912 | G/C | — | — |
| rs370300274 | 17:44,399,698 | C/A | — | uncertain significance |
| rs758187209 | 17:44,399,704 | C/A | — | uncertain significance |
| rs748729606 | 17:44,400,333 | C/G | — | uncertain significance |
| rs2544692584 | 17:44,400,363 | T/A | — | uncertain significance |
| rs2544734994 | 17:44,407,993 | T/C | — | uncertain significance |
| rs1863114 | 17:44,408,004 | A/C | missense variant | — |
| rs2544735877 | 17:44,408,127 | C/G | — | uncertain significance |
| rs1469296892 | 17:44,408,200 | G/A | — | uncertain significance |
| rs778412898 | 17:44,408,247 | G/A | — | likely benign |
| rs1863117 | 17:44,408,262 | A/G | — | uncertain significance |
Showing 100 of 127 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.