ClinVar Miner

Variants in gene ATL1 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: 6
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HGVS dbSNP
NM_001127713.1(ATL1):c.1222A>G (p.Met408Val) rs28939094
NM_001127713.1(ATL1):c.1243C>T (p.Arg415Trp) rs119476050
NM_001127713.1(ATL1):c.467C>T (p.Thr156Ile) rs137852657
NM_001127713.1(ATL1):c.470T>G (p.Leu157Trp) rs119476051
NM_001127713.1(ATL1):c.715C>T (p.Arg239Cys) rs119476046
NM_001127713.1(ATL1):c.773A>G (p.His258Arg) rs119476048

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