ClinVar Miner

Variants in gene HNF1A with conflicting interpretations "likely benign" and "uncertain significance"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 12
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NM_000545.6(HNF1A):c.1015G>A (p.Gly339Ser) rs766790596
NM_000545.6(HNF1A):c.1310-12C>T rs193922579
NM_000545.6(HNF1A):c.1501+6C>T rs374306837
NM_000545.6(HNF1A):c.1502-14T>C rs765596650
NM_000545.6(HNF1A):c.1522G>A (p.Glu508Lys) rs483353044
NM_000545.6(HNF1A):c.1539C>T (p.Thr513=) rs193922584
NM_000545.6(HNF1A):c.1624-15G>A rs193922585
NM_000545.6(HNF1A):c.1624-19G>A rs193922586
NM_000545.6(HNF1A):c.336G>A (p.Pro112=) rs371365341
NM_000545.6(HNF1A):c.92G>A (p.Gly31Asp) rs137853247
NM_000545.6(HNF1A):c.954C>T (p.His318=) rs193922607
NM_000545.6(HNF1A):c.965A>G (p.Tyr322Cys) rs140491072

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