ClinVar Miner

List of variants in gene NDUFS7 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: 9
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NM_024407.5(NDUFS7):c.*3_*5CCG[4] rs3065757
NM_024407.5(NDUFS7):c.*3_*5CCG[5] rs3065757
NM_024407.5(NDUFS7):c.*8G>A rs756081375
NM_024407.5(NDUFS7):c.153C>T (p.Ala51=) rs140236960
NM_024407.5(NDUFS7):c.21T>C (p.Pro7=) rs201222388
NM_024407.5(NDUFS7):c.270C>T (p.Ala90=) rs375120743
NM_024407.5(NDUFS7):c.322G>A (p.Val108Met) rs368174338
NM_024407.5(NDUFS7):c.561C>A (p.Ala187=) rs144570086
NM_024407.5(NDUFS7):c.613C>G (p.Arg205Gly) rs775856806

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