ClinVar Miner

List of variants in gene combination NDUFS8, TCIRG1 reported as benign for bone remodeling disease

Included ClinVar conditions (104):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_002496.4(NDUFS8):c.*14C>T rs1051806 0.18509

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