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rs777692271

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs777692271(C;C)
Make rs777692271(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position67611559
GeneNDUFV1
is asnp
is mentioned by
dbSNPrs777692271
ebirs777692271
HLIrs777692271
Exacrs777692271
Varsomers777692271
Maprs777692271
PheGenIrs777692271
hapmaprs777692271
1000 genomesrs777692271
hgdprs777692271
ensemblrs777692271
gopubmedrs777692271
geneviewrs777692271
scholarrs777692271
googlers777692271
pharmgkbrs777692271
gwascentralrs777692271
openSNPrs777692271
23andMers777692271
23andMe allrs777692271
SNP Nexus

SNPshotrs777692271
SNPdbers777692271
MSV3drs777692271
GWAS Ctlgrs777692271
Max Magnitude0
ClinVar
Risk rs777692271(C;C)
Alt rs777692271(C;C)
Reference rs777692271(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFV1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.67379030T>C
CLNSRC
CLNACC RCV000199113.2,