ClinVar Miner

List of variants reported as likely pathogenic for Pendred syndrome by Fulgent Genetics

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_000441.1(SLC26A4):c.1001G>T (p.Gly334Val) rs146281367
NM_000441.1(SLC26A4):c.2171A>G (p.Asp724Gly) rs757820624
NM_000441.1(SLC26A4):c.706C>G (p.Leu236Val) rs111033242

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