ClinVar Miner

List of variants reported as uncertain significance for autosomal dominant nonsyndromic deafness 6

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 18
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NM_006005.3(WFS1):c.1079G>A (p.Cys360Tyr) rs147157374
NM_006005.3(WFS1):c.1124G>A (p.Arg375His) rs142671083
NM_006005.3(WFS1):c.1167T>G (p.Asp389Glu) rs201282601
NM_006005.3(WFS1):c.1235T>C (p.Val412Ala) rs144951440
NM_006005.3(WFS1):c.1297G>A (p.Ala433Thr) rs138771366
NM_006005.3(WFS1):c.1371G>T (p.Arg457Ser) rs113446173
NM_006005.3(WFS1):c.1396G>A (p.Gly466Ser) rs727503750
NM_006005.3(WFS1):c.1538A>C (p.Tyr513Ser) rs544933961
NM_006005.3(WFS1):c.1633G>A (p.Val545Met) rs201993978
NM_006005.3(WFS1):c.1724C>G (p.Ala575Gly) rs71524360
NM_006005.3(WFS1):c.1846G>T (p.Ala616Ser) rs553336498
NM_006005.3(WFS1):c.1957C>T (p.Arg653Cys) rs201064551
NM_006005.3(WFS1):c.2029G>A (p.Ala677Thr) rs757027394
NM_006005.3(WFS1):c.535G>A (p.Ala179Thr) rs776685250
NM_006005.3(WFS1):c.683G>A (p.Arg228His) rs150771247
NM_006005.3(WFS1):c.716A>G (p.Lys239Arg) rs727503747
NM_006005.3(WFS1):c.728C>T (p.Ala243Val) rs147147660
NM_006005.3(WFS1):c.817G>A (p.Glu273Lys) rs142428158

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