ClinVar Miner

Variants in gene WRN with conflicting interpretations "pathogenic" and "pathogenic"

Submission 1 (pathogenic) minimum review status: Submission 1 (pathogenic) method:
Submission 2 (pathogenic) minimum review status: Submission 2 (pathogenic) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 3
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HGVS dbSNP
NM_000553.4(WRN):c.1105C>T (p.Arg369Ter) rs17847577
NM_000553.4(WRN):c.3139-1G>C rs113993961
NM_000553.4(WRN):c.3590delA (p.Asn1197Thrfs) rs281865160

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