ClinVar Miner

Variants in gene WDR35 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 7
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HGVS dbSNP gnomAD frequency
NM_020779.4(WDR35):c.1601G>A (p.Arg534Gln) rs113345685 0.01206
NM_020779.4(WDR35):c.2262C>T (p.Asp754=) rs147206032 0.00285
NM_020779.4(WDR35):c.318T>C (p.Ile106=) rs115963122 0.00263
NM_020779.4(WDR35):c.355C>T (p.Arg119Cys) rs140308808 0.00221
NM_020779.4(WDR35):c.770T>C (p.Val257Ala) rs142955097 0.00095
NM_020779.4(WDR35):c.2149A>G (p.Ile717Val) rs144493712 0.00089
NM_020779.4(WDR35):c.1058G>C (p.Arg353Pro) rs76623454

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