ClinVar Miner

List of variants in gene IDS reported as uncertain significance 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: 7
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HGVS dbSNP
NC_000023.10:g.(?_148564257)_(148586687_?)dup
NM_000202.8(IDS):c.1264T>C (p.Cys422Arg)
NM_000202.8(IDS):c.1400C>T (p.Pro467Leu)
NM_000202.8(IDS):c.187A>G (p.Asn63Asp)
NM_000202.8(IDS):c.301C>T (p.Arg101Cys) rs782738754
NM_000202.8(IDS):c.331G>C (p.Val111Leu)
NM_000202.8(IDS):c.389C>T (p.Thr130Ile) rs1557340233

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