ClinVar Miner

List of variants in gene NDUFS4 reported as likely benign 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: 2
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HGVS dbSNP
NM_002495.3(NDUFS4):c.424+19dupT rs140172554
NM_002495.4(NDUFS4):c.*46G>A rs567

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