Have questions? Visit https://www.reddit.com/r/SNPedia

rs863224120

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224120(A;A)
Make rs863224120(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position67610487
GeneNDUFV1
is asnp
is mentioned by
dbSNPrs863224120
ebirs863224120
HLIrs863224120
Exacrs863224120
Varsomers863224120
Maprs863224120
PheGenIrs863224120
hapmaprs863224120
1000 genomesrs863224120
hgdprs863224120
ensemblrs863224120
gopubmedrs863224120
geneviewrs863224120
scholarrs863224120
googlers863224120
pharmgkbrs863224120
gwascentralrs863224120
openSNPrs863224120
23andMers863224120
23andMe allrs863224120
SNP Nexus

SNPshotrs863224120
SNPdbers863224120
MSV3drs863224120
GWAS Ctlgrs863224120
Max Magnitude0
ClinVar
Risk rs863224120(A;A)
Alt rs863224120(A;A)
Reference rs863224120(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene NDUFV1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.67377958G>A
CLNSRC
CLNACC RCV000197627.1,