SLC9A1

solute carrier family 9 member A1

Summary

This gene encodes a Na+/H+ antiporter that is a member of the solute carrier family 9. The encoded protein is a plasma membrane transporter that is expressed in the kidney and intestine. This protein plays a central role in regulating pH homeostasis, cell migration and cell volume. This protein may also be involved in tumor growth. [provided by RefSeq, Sep 2011]

Known Variants165 total

rsid	Position (GRCh37)	Alleles	Class	ClinVar
rs4266911	1:27,426,796	T/C	—	benign
rs2523095478	1:27,426,847	G/A	—	uncertain significance
rs148578867	1:27,426,849	G/C	—	likely benign
rs1239594053	1:27,426,853	G/C	—	uncertain significance
rs140754742	1:27,426,875	T/C	—	uncertain significance
rs760629405	1:27,426,889	G/A	—	uncertain significance
rs2124123678	1:27,426,894	G/T	—	uncertain significance
rs539906064	1:27,426,903	C/T	—	likely benign
rs2083133359	1:27,426,927	T/G	—	likely benign
rs750040030	1:27,426,953	G/A	—	uncertain significance
rs140504210	1:27,426,971	C/T	—	uncertain significance
rs149106926	1:27,426,972	G/A	—	likely benign
rs138525900	1:27,426,974	C/T	—	uncertain significance
rs748647066	1:27,426,975	G/A	—	likely benign
rs778021539	1:27,426,980	C/T	—	uncertain significance
rs147966767	1:27,426,987	C/T	—	benign
rs141694580	1:27,427,009	C/T	—	uncertain significance
rs369393494	1:27,427,010	G/A	—	uncertain significance
rs2523096403	1:27,427,019	C/G	—	uncertain significance
rs1359689057	1:27,427,038	C/G	—	uncertain significance
rs4418629	1:27,427,041	T/C	—	benign
rs545801890	1:27,427,065	G/A	—	likely benign
rs745617798	1:27,427,084	G/A	—	uncertain significance
rs1570840726	1:27,427,087	T/C	—	uncertain significance
rs148527788	1:27,427,110	C/T	—	likely benign
rs142887458	1:27,427,117	G/A	—	uncertain significance
rs2523099169	1:27,427,677	C/A	—	likely benign
rs371426452	1:27,427,681	G/A	—	likely benign
rs547605711	1:27,427,701	G/A	—	likely benign
rs2523099274	1:27,427,703	T/C	—	uncertain significance
rs1323099528	1:27,427,712	G/T	—	likely benign
rs201372679	1:27,427,718	T/C	—	benign
rs1047569723	1:27,427,742	C/A	—	uncertain significance
rs200610741	1:27,427,749	C/T	—	likely benign
rs549895277	1:27,427,784	C/T	—	likely benign
rs778795073	1:27,427,786	G/A	—	likely benign
rs76797378	1:27,428,197	A/C	—	benign
rs2083146343	1:27,428,222	C/T	—	conflicting classifications of pathogenicity
rs756321872	1:27,428,233	G/A	—	uncertain significance
rs143101417	1:27,428,276	G/A	—	likely benign
rs374695167	1:27,428,285	T/G	—	likely benign
rs2523101578	1:27,428,286	G/C	—	uncertain significance
rs774782841	1:27,428,314	G/A	—	uncertain significance
rs6598870	1:27,428,321	T/C	—	benign
rs41291060	1:27,428,333	C/T	—	benign
rs764289198	1:27,428,334	G/A	—	likely benign
rs370704524	1:27,428,496	C/T	—	likely benign
rs768169083	1:27,428,531	G/T	—	uncertain significance
rs746382284	1:27,428,547	C/T	—	uncertain significance
rs1309855858	1:27,428,548	G/A	—	uncertain significance
rs2523103500	1:27,428,552	C/A	—	uncertain significance
rs143944969	1:27,428,593	C/T	—	uncertain significance
rs199786766	1:27,428,594	G/C	—	likely benign
rs1392044134	1:27,428,612	G/C	—	uncertain significance
rs139314838	1:27,428,621	C/T	—	likely benign
rs993647773	1:27,428,626	G/A	—	likely benign
rs1030832203	1:27,428,887	G/A	—	likely benign
rs747566604	1:27,428,919	C/A	—	uncertain significance
rs371138291	1:27,428,923	G/A	—	likely benign
rs143340388	1:27,428,932	C/G	—	likely benign
rs373894487	1:27,428,938	G/A	—	likely benign
rs202060037	1:27,428,971	G/T	—	likely benign
rs760631128	1:27,428,983	G/C	—	likely benign
rs144261466	1:27,429,001	G/A	—	conflicting classifications of pathogenicity
rs759143875	1:27,429,151	G/T	—	likely benign
rs557797010	1:27,429,178	G/A	—	likely benign
rs2523107727	1:27,429,184	A/G	—	likely benign
rs745927136	1:27,429,225	G/A	—	uncertain significance
rs200289352	1:27,429,241	G/C	—	likely benign
rs866445773	1:27,429,733	T/C	—	uncertain significance
rs756135813	1:27,429,747	C/T	—	likely benign
rs902869080	1:27,429,748	G/A	—	uncertain significance
rs2523110612	1:27,429,767	C/G	—	uncertain significance
rs11577385	1:27,429,807	G/C	—	likely benign
rs2083161189	1:27,429,819	G/C	—	likely benign
rs150015600	1:27,432,319	C/T	—	likely benign
rs1308941023	1:27,432,388	G/A	—	likely benign
rs2124137046	1:27,432,437	G/C	—	uncertain significance
rs199663689	1:27,432,454	C/T	—	likely benign
rs797044991	1:27,432,470	G/A	—	uncertain significance
rs2523120782	1:27,432,482	G/T	—	uncertain significance
rs35607809	1:27,432,505	G/A	—	likely benign
rs1334434379	1:27,432,508	G/A	—	likely benign
rs1553175089	1:27,432,510	T/G	—	likely pathogenic
rs752840548	1:27,432,538	G/C	—	uncertain significance
rs765187776	1:27,432,539	A/G	—	uncertain significance
rs2523121140	1:27,432,580	T/C	—	uncertain significance
rs1410044158	1:27,432,585	G/T	—	likely benign
rs2083182711	1:27,432,596	G/T	—	likely benign
rs1455459442	1:27,434,129	T/A	—	likely benign
rs1284168040	1:27,434,148	G/A	—	uncertain significance
rs543760155	1:27,434,200	G/A	—	likely benign
rs755603773	1:27,434,209	G/A	—	likely benign
rs368704142	1:27,434,215	C/T	—	likely benign
rs138422424	1:27,434,224	G/A	—	likely benign
rs547467847	1:27,434,227	G/A	—	likely benign
rs757722296	1:27,434,251	G/A	—	likely benign
rs2124142438	1:27,434,309	A/G	—	uncertain significance
rs2523130203	1:27,434,368	A/G	—	likely benign
rs539531871	1:27,434,373	C/T	—	benign

Showing 100 of 165 variants. Use the SNP search for the full list.

Gene information from NCBI Gene. Variant classifications from ClinVar.