ClinVar Miner

List of variants in gene WHRN reported as benign for auditory system disease

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 24
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NM_015404.4(WHRN):c.-257C>G rs73555447
NM_015404.4(WHRN):c.-295C>G rs7861589
NM_015404.4(WHRN):c.-391C>A rs4527950
NM_015404.4(WHRN):c.-510G>A rs10759714
NM_015404.4(WHRN):c.-91C>T rs2297814
NM_015404.4(WHRN):c.1091= (p.His364=) rs10817610
NM_015404.4(WHRN):c.117G>A (p.Val39=) rs2297815
NM_015404.4(WHRN):c.1318G>A (p.Ala440Thr) rs4978584
NM_015404.4(WHRN):c.1352G>A (p.Gly451Asp) rs117352600
NM_015404.4(WHRN):c.1353T>C (p.Gly451=) rs4979387
NM_015404.4(WHRN):c.1515G>A (p.Ala505=) rs34252199
NM_015404.4(WHRN):c.1627-12G>A rs2274160
NM_015404.4(WHRN):c.1684C>G (p.Pro562Ala) rs12339210
NM_015404.4(WHRN):c.1838T>C (p.Met613Thr) rs942519
NM_015404.4(WHRN):c.2256= (p.Gln752=) rs6478078
NM_015404.4(WHRN):c.2283C>T (p.Ser761=) rs34963246
NM_015404.4(WHRN):c.229A>T (p.Thr77Ser) rs56204273
NM_015404.4(WHRN):c.2348T>C (p.Val783Ala) rs2274159
NM_015404.4(WHRN):c.2388C>A (p.Asn796Lys) rs2274158
NM_015404.4(WHRN):c.2586C>A (p.His862Gln) rs117592152
NM_015404.4(WHRN):c.33C>G (p.Ser11Arg) rs45527543

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