Autosomal Recessive Nonsyndromic Hearing Loss 4

Other 385 variants 3 genes

Upload your DNA to see your personal risk score for Autosomal Recessive Nonsyndromic Hearing Loss 4.

Associated Genes (3)

SLC26A4 SLC26A4-AS1;SLC26A4 KCNJ10

Associated Variants (385)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS1584337274	SLC26A4	—	—	exploratory
RS1584337228	SLC26A4	—	—	exploratory
RS1584304377	SLC26A4	—	—	exploratory
RS111033316	SLC26A4	—	—	strong
RS200511789	SLC26A4	—	—	strong
RS397516411	SLC26A4-AS1;SLC26A4	—	—	strong
RS111033314	SLC26A4	—	—	strong
RS397516413	SLC26A4	—	—	strong
RS111033305	SLC26A4	—	—	strong
RS111033220	SLC26A4	—	—	strong
RS111033311	SLC26A4	—	—	strong
RS111033306	SLC26A4	—	—	strong
RS397516416	SLC26A4	—	—	strong
RS397516417	SLC26A4	—	—	strong
RS111033407	SLC26A4	—	—	strong
RS397516418	SLC26A4	—	—	strong
RS137853074	KCNJ10	—	—	strong
RS7811324	SLC26A4	—	—	strong
RS111033312	SLC26A4	—	—	strong
RS397516420	SLC26A4	—	—	strong
RS397516421	SLC26A4	—	—	strong
RS111033200	SLC26A4	—	—	strong
RS111033423	SLC26A4	—	—	strong
RS55638457	SLC26A4	—	—	strong
RS1406937547	SLC26A4	—	—	strong
RS111033348	SLC26A4	—	—	strong
RS111033308	SLC26A4	—	—	strong
RS80338848	SLC26A4	—	—	strong
RS28939086	SLC26A4	—	—	strong
RS80338849	SLC26A4	—	—	strong
RS111033244	SLC26A4	—	—	strong
RS111033303	SLC26A4	—	—	strong
RS121908361	SLC26A4	—	—	strong
RS121908364	SLC26A4	—	—	strong
RS121908362	SLC26A4	—	—	strong
RS121908363	SLC26A4	—	—	strong
RS765884316	SLC26A4	—	—	strong
RS111033307	SLC26A4	—	—	strong
RS1584317722	SLC26A4	—	—	strong
RS2129315781	SLC26A4	—	—	strong
RS121908365	SLC26A4	—	—	strong
RS111033199	SLC26A4	—	—	strong
RS111033254	SLC26A4	—	—	strong
RS111033205	SLC26A4	—	—	strong
RS111033313	SLC26A4	—	—	strong
RS121908366	SLC26A4	—	—	strong
RS111033212	SLC26A4	—	—	strong
RS137853067	KCNJ10	—	—	strong
RS137853070	KCNJ10	—	—	strong
RS137853073	KCNJ10	—	—	strong

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