ClinVar Miner

List of variants in gene combination AMMECR1, RTL9 reported as 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: 1
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HGVS dbSNP
NC_000023.11:g.110250890_110665082del

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