Sensorineural Hearing Loss Disorder

Other 53 variants 36 genes

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Associated Genes (36)

TMC1 CDC14A KARS1 GGPS1 SLC12A2 AFG3L2 RRM2B MYO7A COL9A1 ATP6V0A4 SLC52A2 NARS2 CLDN14 MYO3A MRPS7 SLC26A4 STX4 ZSCAN10 MYO15A SPNS2 CDH23 SLC19A2 USH2A EDN3 TMIE MT-TL1 HGF GJB2 NEFL HARS2 CEP78 COL11A2 AIFM1 TECTA LMX1A KCNE1

Associated Variants (53)

RSID	Gene	Risk Allele	Odds Ratio	Evidence
RS1181901214	TMC1	—	—	strong
RS1571346132	CDC14A	—	—	strong
RS1415687857	KARS1	—	—	strong
RS1262402879	GGPS1	—	—	strong
RS1581138965	SLC12A2	—	—	strong
RS1908371616	AFG3L2	—	—	strong
RS1810682433	RRM2B	—	—	strong
RS1407313220	MYO7A	—	—	strong
RS2127544065	COL9A1	—	—	strong
RS746982385	ATP6V0A4	—	—	strong
RS1554854341	SLC52A2	—	—	strong
RS953849956	NARS2	—	—	strong
RS2146412304	CLDN14	—	—	strong
RS760866131	MYO3A	—	—	strong
RS752619610	MRPS7	—	—	strong
RS2129311933	SLC26A4	—	—	strong
RS763815427	STX4	—	—	strong
RS756738709	ZSCAN10	—	—	strong
RS1303325551	ZSCAN10	—	—	strong
RS2142436821	MYO15A	—	—	strong
RS1905545130	SPNS2	—	—	strong
RS2545055011	MRPS7	—	—	strong
RS2494385418	CDH23	—	—	strong
RS1658539563	SLC19A2	—	—	strong
RS2527813410	USH2A	—	—	strong
RS745795470	EDN3	—	—	strong
RS28942096	TMIE	—	—	strong
RS28942097	TMIE	—	—	strong
RS199474657	MT-TL1	—	—	strong
RS1788701297	HGF	—	—	strong
RS80338944	GJB2	—	—	strong
RS104894396	GJB2	—	—	strong
RS104894403	GJB2	—	—	strong
RS28931594	GJB2	—	—	strong
RS58982919	NEFL	—	—	strong
RS111033256	SLC26A4	—	—	strong
RS150529554	GJB2	—	—	strong
RS200089613	HARS2	—	—	strong
RS876661301	TMIE	—	—	strong
RS1057517694	CEP78	—	—	strong
RS1057517695	CEP78	—	—	strong
RS745434198	COL11A2	—	—	strong
RS1057518895	AIFM1	—	—	strong
RS756147087	CDH23	—	—	strong
RS772606235	TECTA	—	—	strong
RS763320093	LMX1A	—	—	strong
RS1244688796	KCNE1	—	—	strong
RS1567498374	KARS1	—	—	strong
RS1581536078	HARS2	—	—	strong
RS1581550832	HARS2	—	—	strong

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