ClinVar Miner

Variants in gene WFS1 with conflicting interpretations "uncertain significance" and "likely pathogenic"

Submission 1 (uncertain significance) minimum review status: Submission 1 (uncertain significance) method:
Submission 2 (likely pathogenic) minimum review status: Submission 2 (likely pathogenic) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 8
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HGVS dbSNP
NM_006005.3(WFS1):c.1037C>T (p.Pro346Leu) rs773900146
NM_006005.3(WFS1):c.1672C>T (p.Arg558Cys) rs199946797
NM_006005.3(WFS1):c.1831_1832delinsTA (p.Arg611Tyr) rs863224266
NM_006005.3(WFS1):c.1886G>A (p.Arg629Gln) rs146670741
NM_006005.3(WFS1):c.2020G>A (p.Gly674Arg) rs200672755
NM_006005.3(WFS1):c.2195G>A (p.Arg732His) rs149013740
NM_006005.3(WFS1):c.2603G>A (p.Arg868His) rs56393026
NM_006005.3(WFS1):c.911_914dup (p.Met306_Ala307insTer) rs863224264

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