CSMD2

CUB and Sushi multiple domains 2

Summary

The protein encoded by this gene is thought to be involved in the control of complement cascade of the immune system. Defects in this gene have been associated with schizophrenia. This gene may act as a tumor suppressor for colorectal cancer. [provided by RefSeq, Jan 2020]

Known Variants216 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs10798959	1:33,983,019	C/A	—	—
rs772977995	1:33,985,151	C/G	—	uncertain significance
rs1654062402	1:33,985,161	C/G	—	likely benign
rs201053172	1:33,985,191	C/T	missense variant	—
rs780673057	1:33,985,195	C/T	—	uncertain significance
rs1463989820	1:33,985,218	G/A	—	uncertain significance
rs763420853	1:33,985,263	A/T	—	uncertain significance
rs151161296	1:33,985,275	C/G	—	uncertain significance
rs1051073009	1:33,985,500	A/C	—	uncertain significance
rs746146936	1:33,987,078	C/T	—	uncertain significance
rs1191250430	1:33,987,080	A/G	—	uncertain significance
rs747298393	1:33,987,086	C/T	—	uncertain significance
rs1184664313	1:33,988,960	C/T	—	uncertain significance
rs1386651390	1:33,990,545	C/A	—	uncertain significance
rs2523301594	1:33,990,578	G/T	—	uncertain significance
rs148333754	1:33,990,586	C/T	—	uncertain significance
rs139653382	1:33,990,638	C/A	—	uncertain significance
rs1384106253	1:33,992,819	T/G	—	uncertain significance
rs149656829	1:33,992,823	G/A	—	uncertain significance
rs148437366	1:33,992,852	C/T	—	likely benign
rs146169512	1:33,998,798	C/T	—	likely benign
rs189523744	1:33,998,799	G/A	—	uncertain significance
rs180811686	1:33,998,805	G/A	—	uncertain significance
rs146010136	1:33,999,413	G/T	—	uncertain significance
rs200031290	1:34,002,631	C/G	—	uncertain significance
rs1479653968	1:34,003,131	G/A	—	uncertain significance
rs374554934	1:34,003,147	A/G	—	uncertain significance
rs151250469	1:34,003,162	C/T	—	uncertain significance
rs778281288	1:34,003,198	C/T	—	uncertain significance
rs780786759	1:34,006,254	C/A	—	uncertain significance
rs769571705	1:34,006,265	T/C	—	uncertain significance
rs139840174	1:34,006,739	C/A	—	uncertain significance
rs767117766	1:34,006,812	G/A	—	likely benign
rs142484997	1:34,006,857	A/T	—	uncertain significance
rs1387687859	1:34,006,873	C/A	—	uncertain significance
rs893582249	1:34,008,361	G/A	—	uncertain significance
rs2523437381	1:34,008,385	G/A	—	uncertain significance
rs554466777	1:34,008,416	C/A	—	uncertain significance
rs780884054	1:34,011,658	C/T	—	uncertain significance
rs4424471	1:34,011,692	T/G	—	benign
rs751920658	1:34,011,709	C/T	—	uncertain significance
rs753247221	1:34,011,726	C/A	—	uncertain significance
rs368320095	1:34,011,732	C/T	—	uncertain significance
rs775463572	1:34,011,768	C/G	—	uncertain significance
rs199535455	1:34,011,799	C/T	—	uncertain significance
rs764723077	1:34,015,848	G/A	—	uncertain significance
rs370638892	1:34,015,858	C/T	—	uncertain significance
rs548133161	1:34,023,261	T/C	—	—
rs28438078	1:34,024,672	G/A	intron variant	—
rs771472015	1:34,033,195	A/C	—	uncertain significance
rs776112521	1:34,033,300	C/T	—	uncertain significance
rs923953707	1:34,035,049	A/G	—	uncertain significance
rs763199591	1:34,035,082	C/G	—	uncertain significance
rs149425378	1:34,035,105	C/A	—	uncertain significance
rs777939906	1:34,035,117	G/C	—	uncertain significance
rs1441783388	1:34,037,156	C/T	—	uncertain significance
rs765477684	1:34,037,261	T/G	—	uncertain significance
rs193921034	1:34,037,281	C/A	—	uncertain significance
rs138705399	1:34,037,294	C/T	—	uncertain significance
rs778412668	1:34,038,130	G/A	—	uncertain significance
rs1457386505	1:34,038,147	G/A	—	uncertain significance
rs770489446	1:34,038,148	T/C	—	uncertain significance
rs2523691325	1:34,038,201	C/T	—	uncertain significance
rs1175420638	1:34,038,222	G/T	—	uncertain significance
rs138161656	1:34,042,937	T/C	—	uncertain significance
rs146054660	1:34,042,986	C/T	—	uncertain significance
rs1638352036	1:34,042,991	T/C	—	uncertain significance
rs958161891	1:34,043,057	G/A	—	uncertain significance
rs190368073	1:34,046,406	C/T	—	uncertain significance
rs1315541093	1:34,046,440	T/C	—	uncertain significance
rs372170838	1:34,049,389	C/T	—	uncertain significance
rs2523800261	1:34,049,428	G/A	—	uncertain significance
rs200540649	1:34,052,119	G/A	—	uncertain significance
rs2523825930	1:34,052,213	G/T	—	likely benign
rs1557579687	1:34,052,214	T/A	—	uncertain significance
rs143826784	1:34,052,715	C/T	—	uncertain significance
rs781114510	1:34,052,718	C/A	—	uncertain significance
rs773952980	1:34,066,491	C/A	—	uncertain significance
rs140769172	1:34,066,566	C/T	—	likely benign
rs1359228096	1:34,067,979	T/C	—	uncertain significance
rs144426100	1:34,068,024	G/A	—	uncertain significance
rs766482245	1:34,068,038	A/G	—	uncertain significance
rs573603633	1:34,068,042	G/A	—	uncertain significance
rs1640295809	1:34,068,116	T/G	—	uncertain significance
rs370588035	1:34,068,135	C/T	—	uncertain significance
rs143860895	1:34,068,136	G/A	—	likely benign
rs781096021	1:34,070,968	G/A	—	uncertain significance
rs777207927	1:34,071,025	C/G	—	uncertain significance
rs200429573	1:34,071,067	T/C	—	uncertain significance
rs142786319	1:34,071,492	T/C	—	uncertain significance
rs143724889	1:34,071,493	A/G	—	uncertain significance
rs750582845	1:34,071,499	C/T	—	uncertain significance
rs769171132	1:34,071,505	C/T	—	uncertain significance
rs774016459	1:34,071,523	T/C	—	uncertain significance
rs202113840	1:34,071,533	C/G	—	uncertain significance
rs370723530	1:34,071,543	T/C	—	uncertain significance
rs367864010	1:34,076,653	G/C	—	uncertain significance
rs545062582	1:34,076,714	C/T	—	likely benign
rs764362857	1:34,076,742	C/T	—	likely benign
rs201628546	1:34,076,772	G/A	—	uncertain significance

Showing 100 of 216 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.