CAND1.11

uncharacterized LOC100130460

Known Variants30 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs4910118	11:10,329,685	C/T	regulatory region variant	—
rs4444073	11:10,331,664	A/C	regulatory region variant	—
rs11042731	11:10,340,423	C/T	intron variant	—
rs7129220	11:10,350,538	G/A	regulatory region variant	—
rs2957683	11:10,352,175	C/G	regulatory region variant	—
rs2084600	11:10,352,295	A/G	intron variant	—
rs1450271	11:10,356,115	C/T	intron variant	—
rs11599958	11:10,358,095	C/T	intron variant	—
rs2403309	11:10,358,139	A/T	intron variant	—
rs7925720	11:10,358,540	G/A	intron variant	—
rs7944291	11:10,358,628	T/C	—	—
rs7944299	11:10,358,655	T/C	—	—
rs4494298	11:10,363,157	A/G	intron variant	—
rs2957688	11:10,364,963	G/A	intron variant	—
rs9704692	11:10,366,029	C/T	intron variant	—
rs2957689	11:10,367,754	G/T	—	—
rs2957692	11:10,368,119	A/G	intron variant	—
rs2957694	11:10,369,014	G/A	intron variant	—
rs1580006	11:10,370,675	A/T	regulatory region variant	—
rs182264490	11:10,373,076	G/C	regulatory region variant	—
rs2923078	11:10,381,766	A/G	—	—
rs2860284	11:10,386,476	T/C	intron variant	—
rs2923084	11:10,388,782	A/G	regulatory region variant	—
rs6484218	11:10,390,581	G/A	intron variant	—
rs2957664	11:10,398,306	G/A	intron variant	—
rs2923120	11:10,400,414	C/T	regulatory region variant	—
rs2957668	11:10,404,382	T/G	—	—
rs12226039	11:10,406,464	T/C	—	—
rs11042773	11:10,406,687	C/T	intron variant	—
rs11042800	11:10,450,588	C/T	intron variant	—

Gene information from NCBI Gene. Variant classifications from ClinVar.