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rs767602961

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767602961(A;A)
Make rs767602961(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position67609604
GeneNDUFV1
is asnp
is mentioned by
dbSNPrs767602961
ebirs767602961
HLIrs767602961
Exacrs767602961
Varsomers767602961
Maprs767602961
PheGenIrs767602961
hapmaprs767602961
1000 genomesrs767602961
hgdprs767602961
ensemblrs767602961
gopubmedrs767602961
geneviewrs767602961
scholarrs767602961
googlers767602961
pharmgkbrs767602961
gwascentralrs767602961
openSNPrs767602961
23andMers767602961
23andMe allrs767602961
SNP Nexus

SNPshotrs767602961
SNPdbers767602961
MSV3drs767602961
GWAS Ctlgrs767602961
Max Magnitude0
ClinVar
Risk rs767602961(A;A)
Alt rs767602961(A;A)
Reference rs767602961(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFV1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.67377075G>A
CLNSRC
CLNACC RCV000199260.1,