ClinVar Miner

List of variants in gene combination LIAS, LOC112939935 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: 5
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NM_006859.4(LIAS):c.23C>T (p.Ala8Val)
NM_006859.4(LIAS):c.29G>A (p.Arg10His) rs1370681479
NM_006859.4(LIAS):c.35T>A (p.Leu12Gln) rs1436660040
NM_006859.4(LIAS):c.37G>A (p.Gly13Arg) rs1320749254

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