ClinVar Miner

List of variants studied for Wolfram-like syndrome

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 24
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HGVS dbSNP
NM_004667.5(HERC2):c.7617+4A>C rs1567006110
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.124C>T (p.Arg42Ter) rs71530923
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.1957C>T (p.Arg653Cys) rs201064551
NM_006005.3(WFS1):c.2029G>A (p.Ala677Thr) rs757027394
NM_006005.3(WFS1):c.2051C>T (p.Ala684Val) rs387906930
NM_006005.3(WFS1):c.2338G>A (p.Gly780Ser) rs387906931
NM_006005.3(WFS1):c.2425G>A (p.Glu809Lys) rs71539673
NM_006005.3(WFS1):c.2590G>A (p.Glu864Lys) rs74315205
NM_006005.3(WFS1):c.482G>A (p.Arg161Gln) rs115346085
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
WFS1, ARG228GLN
WFS1, LYS836ASN

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