SLC4A3

solute carrier family 4 member 3

Summary

The protein encoded by this gene is a plasma membrane anion exchange protein. The encoded protein has been found in brain, heart, kidney, small intestine, and lung. [provided by RefSeq, May 2016]

Known Variants123 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs897296053	2:220,492,737	C/T	—	uncertain significance
rs200005603	2:220,492,742	G/A	—	uncertain significance
rs2469257030	2:220,493,148	C/A	—	uncertain significance
rs200942352	2:220,493,149	C/G	—	uncertain significance
rs387907529	2:220,493,221	A/G	—	uncertain significance
rs73072582	2:220,493,236	C/T	—	likely benign
rs750702521	2:220,493,275	G/A	—	uncertain significance
rs41272705	2:220,493,861	C/T	—	likely benign
rs1192826246	2:220,493,872	G/A	—	uncertain significance
rs755835363	2:220,493,910	C/T	—	uncertain significance
rs766023665	2:220,493,949	A/C	—	uncertain significance
rs184135231	2:220,493,958	C/T	—	likely benign
rs139947594	2:220,493,959	G/A	—	likely benign
rs2106181222	2:220,494,000	C/T	—	uncertain significance
rs148716690	2:220,494,008	C/T	—	likely benign
rs387907531	2:220,494,019	C/T	—	uncertain significance
rs140733778	2:220,494,035	G/A	—	likely benign
rs372011999	2:220,494,036	G/C	—	uncertain significance
rs200923264	2:220,494,042	G/A	—	uncertain significance
rs528947239	2:220,494,112	C/G	—	uncertain significance
rs2469263192	2:220,494,114	C/A	—	uncertain significance
rs549219468	2:220,494,117	C/T	—	uncertain significance
rs597306	2:220,494,118	A/C	—	benign
rs372108403	2:220,494,151	C/T	—	likely benign
rs1698847121	2:220,494,347	A/G	—	uncertain significance
rs773948874	2:220,494,375	C/T	—	conflicting classifications of pathogenicity
rs1197072744	2:220,494,831	G/A	—	uncertain significance
rs138184188	2:220,494,849	C/T	—	likely benign
rs2469268803	2:220,494,853	G/A	—	uncertain significance
rs143751613	2:220,494,859	T/C	—	likely benign
rs780617270	2:220,494,882	A/C	—	uncertain significance
rs146593729	2:220,494,909	G/A	—	uncertain significance
rs387907530	2:220,494,927	C/A	—	uncertain significance
rs761158856	2:220,494,935	C/G	—	uncertain significance
rs387907532	2:220,494,944	C/T	—	uncertain significance
rs1219725773	2:220,494,996	G/C	—	uncertain significance
rs612078	2:220,495,167	A/C	—	benign
rs186106299	2:220,496,187	G/A	—	benign
rs377314291	2:220,496,750	C/T	—	uncertain significance
rs753663643	2:220,496,758	G/A	—	uncertain significance
rs140021661	2:220,496,794	C/T	—	uncertain significance
rs145824315	2:220,496,795	G/A	—	uncertain significance
rs2469278980	2:220,496,828	G/C	—	uncertain significance
rs145141849	2:220,496,989	C/T	—	likely benign
rs41272707	2:220,497,040	G/A	—	benign
rs369812780	2:220,497,045	C/T	—	uncertain significance
rs2469281007	2:220,497,051	G/A	—	pathogenic
rs374698562	2:220,497,117	C/T	—	uncertain significance
rs998353436	2:220,497,129	G/A	—	uncertain significance
rs761799917	2:220,497,158	G/A	—	uncertain significance
rs115885893	2:220,497,682	C/A	—	likely benign
rs35138558	2:220,497,702	C/T	—	benign
rs369274440	2:220,497,736	C/T	—	likely benign
rs748356003	2:220,498,006	G/A	—	uncertain significance
rs761000199	2:220,498,034	G/A	—	uncertain significance
rs759093832	2:220,498,041	A/G	—	likely benign
rs762597778	2:220,498,061	C/T	—	uncertain significance
rs542246311	2:220,498,089	C/T	—	likely benign
rs2469289045	2:220,498,174	A/G	—	uncertain significance
rs2289782	2:220,498,350	G/C	—	benign
rs2469291387	2:220,498,626	G/A	—	uncertain significance
rs370441322	2:220,499,174	G/A	—	uncertain significance
rs151023127	2:220,499,180	G/A	—	uncertain significance
rs144812298	2:220,499,190	A/G	—	likely benign
rs138294583	2:220,499,233	G/A	—	likely benign
rs2469295468	2:220,499,264	A/G	—	uncertain significance
rs144951762	2:220,499,287	C/T	—	likely benign
rs377401064	2:220,500,027	G/A	—	uncertain significance
rs143970704	2:220,500,053	G/A	—	uncertain significance
rs747034568	2:220,500,085	G/A	—	likely benign
rs553891640	2:220,500,088	C/T	—	likely benign
rs781271998	2:220,500,179	G/A	—	uncertain significance
rs1039170052	2:220,500,192	G/A	—	likely benign
rs2469302313	2:220,500,206	G/A	—	uncertain significance
rs140440972	2:220,500,208	C/A	—	benign
rs2305055	2:220,500,321	C/G	—	benign
rs55910611	2:220,500,412	G/A	—	likely benign
rs772630989	2:220,500,425	C/T	—	uncertain significance
rs639214	2:220,500,426	G/A	—	benign
rs759168094	2:220,500,455	C/T	—	uncertain significance
rs142497429	2:220,500,461	C/T	—	uncertain significance
rs2469304231	2:220,500,470	G/A	—	uncertain significance
rs1254650443	2:220,500,524	G/A	—	uncertain significance
rs35394392	2:220,500,830	G/C	—	benign
rs111434009	2:220,501,055	C/T	—	benign
rs113725667	2:220,501,064	C/T	—	likely benign
rs387907533	2:220,501,065	G/A	—	uncertain significance
rs748857141	2:220,501,074	G/A	—	uncertain significance
rs61729099	2:220,501,082	C/T	—	benign
rs780678809	2:220,501,162	C/G	—	uncertain significance
rs755460816	2:220,501,471	G/A	—	uncertain significance
rs775610088	2:220,501,520	C/T	—	uncertain significance
rs2469311274	2:220,501,583	A/G	—	uncertain significance
rs623851	2:220,502,043	T/C	—	benign
rs1222222783	2:220,502,344	G/C	—	uncertain significance
rs61729101	2:220,502,366	G/C	—	likely benign
rs635311	2:220,502,367	A/C	—	benign
rs61729100	2:220,502,407	C/T	—	benign
rs140581019	2:220,502,408	G/A	—	conflicting classifications of pathogenicity
rs781201150	2:220,502,447	C/G	—	uncertain significance

Showing 100 of 123 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.