ClinVar Miner

List of variants in gene combination DLAT, PIH1D2 reported as likely benign for X-linked disease

Included ClinVar conditions (313):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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NM_001931.5(DLAT):c.*1109C>T rs75608010
NM_001931.5(DLAT):c.*873T>C rs73568056
NM_001931.5(DLAT):c.*96C>A rs534753

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