ClinVar Miner

List of variants in gene combination LOC112552175, NDUFA11 reported as uncertain significance for X-linked syndromic intellectual disability

Included ClinVar conditions (163):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 7
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HGVS dbSNP
NM_175614.4(NDUFA11):c.-143C>G rs550697802
NM_175614.4(NDUFA11):c.-201_-200delCT rs759857076
NM_175614.4(NDUFA11):c.-210T>C rs886054650
NM_175614.4(NDUFA11):c.-234T>C rs115530541
NM_175614.4(NDUFA11):c.-31G>A rs886054648
NM_175614.4(NDUFA11):c.-51T>G rs886054649
NM_175614.4(NDUFA11):c.-83G>C rs562075121

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