ClinVar Miner

List of variants in gene NDUFS8 reported as likely pathogenic for Leigh syndrome

Included ClinVar conditions (9):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_002496.4(NDUFS8):c.236C>T (p.Pro79Leu) rs28939679
NM_002496.4(NDUFS8):c.343A>G (p.Lys115Glu) rs764276946
NM_002496.4(NDUFS8):c.441G>C (p.Met147Ile) rs1267554976

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