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

rs35263902

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs35263902(C;T)
Make rs35263902(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome12
Position4654828
GeneNDUFA9
is asnp
is mentioned by
dbSNPrs35263902
ebirs35263902
HLIrs35263902
Exacrs35263902
Varsomers35263902
Maprs35263902
PheGenIrs35263902
hapmaprs35263902
1000 genomesrs35263902
hgdprs35263902
ensemblrs35263902
gopubmedrs35263902
geneviewrs35263902
scholarrs35263902
googlers35263902
pharmgkbrs35263902
gwascentralrs35263902
openSNPrs35263902
23andMers35263902
23andMe allrs35263902
SNP Nexus

SNPshotrs35263902
SNPdbers35263902
MSV3drs35263902
GWAS Ctlgrs35263902
Max Magnitude0
ClinVar
Risk rs35263902(A,T;A,T)
Alt rs35263902(A,T;A,T)
Reference rs35263902(C;C)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene NDUFA9
CLNDBN not provided not specified
Reversed 1
HGVS NC_000012.11:g.4763994G>A; NC_000012.11:g.4763994G>T
CLNSRC
CLNACC RCV000197597.1, RCV000200129.2, RCV000203115.1,