ClinVar Miner

List of variants in gene combination APIP, PDHX reported as uncertain significance for X-linked syndromic intellectual disability

Included ClinVar conditions (165):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 4
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HGVS dbSNP
NM_001166158.1(PDHX):c.-271G>T rs780153979
NM_015957.4(APIP):c.-14C>T rs886048245
NM_015957.4(APIP):c.-18G>A rs761199870
NM_015957.4(APIP):c.-1C>T rs774565620

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