ClinVar Miner

List of variants in gene IDS reported as likely pathogenic 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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HGVS dbSNP
NM_000202.8(IDS):c.133G>C (p.Asp45His) rs869025301
NM_000202.8(IDS):c.143G>C (p.Arg48Pro) rs1569560528
NM_000202.8(IDS):c.1478G>C (p.Arg493Pro)
NM_000202.8(IDS):c.1563A>T (p.Glu521Asp)
NM_000202.8(IDS):c.359C>G (p.Pro120Arg)

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