ClinVar Miner

List of variants reported as uncertain significance for Pendred syndrome by Fulgent Genetics,Fulgent Genetics

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 6
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NM_000441.2(SLC26A4):c.2009T>C (p.Val670Ala) rs200712253
NM_000441.2(SLC26A4):c.2291C>T (p.Thr764Met) rs150597240
NM_002241.5(KCNJ10):c.1043G>A (p.Arg348His) rs146396982
NM_002241.5(KCNJ10):c.1051G>A (p.Asp351Asn) rs373899425
NM_002241.5(KCNJ10):c.511C>T (p.Arg171Trp) rs769666695
NM_002241.5(KCNJ10):c.652C>T (p.Leu218Phe) rs558502886

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