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rs863224118

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224118(A;C)
Make rs863224118(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position67611948
GeneNDUFV1
is asnp
is mentioned by
dbSNPrs863224118
ebirs863224118
HLIrs863224118
Exacrs863224118
Varsomers863224118
Maprs863224118
PheGenIrs863224118
hapmaprs863224118
1000 genomesrs863224118
hgdprs863224118
ensemblrs863224118
gopubmedrs863224118
geneviewrs863224118
scholarrs863224118
googlers863224118
pharmgkbrs863224118
gwascentralrs863224118
openSNPrs863224118
23andMers863224118
23andMe allrs863224118
SNP Nexus

SNPshotrs863224118
SNPdbers863224118
MSV3drs863224118
GWAS Ctlgrs863224118
Max Magnitude0
ClinVar
Risk rs863224118(C;C)
Alt rs863224118(C;C)
Reference rs863224118(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene NDUFV1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.67379419A>C
CLNSRC
CLNACC RCV000197501.1,