ClinVar Miner

List of variants in gene combination DLAT, PIH1D2 reported as benign for X-linked syndromic intellectual disability

Included ClinVar conditions (168):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_001931.4(DLAT):c.*1232_*1235dupAGGA rs368743837
NM_001931.4(DLAT):c.*1248G>C rs9822
NM_001931.4(DLAT):c.*419A>G rs9371

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