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rs762235847

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs762235847(C;T)
Make rs762235847(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position124543167
GeneNDUFB9
is asnp
is mentioned by
dbSNPrs762235847
ebirs762235847
HLIrs762235847
Exacrs762235847
Varsomers762235847
Maprs762235847
PheGenIrs762235847
hapmaprs762235847
1000 genomesrs762235847
hgdprs762235847
ensemblrs762235847
gopubmedrs762235847
geneviewrs762235847
scholarrs762235847
googlers762235847
pharmgkbrs762235847
gwascentralrs762235847
openSNPrs762235847
23andMers762235847
23andMe allrs762235847
SNP Nexus

SNPshotrs762235847
SNPdbers762235847
MSV3drs762235847
GWAS Ctlgrs762235847
Max Magnitude0
ClinVar
Risk rs762235847(G,T;G,T)
Alt rs762235847(G,T;G,T)
Reference rs762235847(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFB9
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.125555408C>T
CLNSRC
CLNACC RCV000198785.1,