ClinVar Miner

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

Included ClinVar conditions (549):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
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HGVS dbSNP
NM_015404.4(WHRN):c.*37C>G rs549195233
NM_015404.4(WHRN):c.*51C>T
NM_015404.4(WHRN):c.-257C>G rs73555447
NM_015404.4(WHRN):c.-295C>G rs7861589
NM_015404.4(WHRN):c.-314C>T
NM_015404.4(WHRN):c.-608_-601del rs150944893
NM_015404.4(WHRN):c.1352G>A (p.Gly451Asp) rs117352600
NM_015404.4(WHRN):c.1515G>A (p.Ala505=) rs34252199
NM_015404.4(WHRN):c.2046G>C (p.Arg682=) rs35258467
NM_015404.4(WHRN):c.2307C>T (p.Gly769=)
NM_015404.4(WHRN):c.2439G>A (p.Thr813=) rs61743618
NM_015404.4(WHRN):c.2586C>A (p.His862Gln) rs117592152
NM_015404.4(WHRN):c.667C>T (p.Arg223Cys) rs76593842
NM_015404.4(WHRN):c.668G>A (p.Arg223His) rs146273185
NM_015404.4(WHRN):c.933A>C (p.Pro311=) rs569159249

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