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rs142609245

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs142609245(C;C)
Make rs142609245(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome2
Position201078946
GeneNDUFB3
is asnp
is mentioned by
dbSNPrs142609245
ebirs142609245
HLIrs142609245
Exacrs142609245
Varsomers142609245
Maprs142609245
PheGenIrs142609245
hapmaprs142609245
1000 genomesrs142609245
hgdprs142609245
ensemblrs142609245
gopubmedrs142609245
geneviewrs142609245
scholarrs142609245
googlers142609245
pharmgkbrs142609245
gwascentralrs142609245
openSNPrs142609245
23andMers142609245
23andMe allrs142609245
SNP Nexus

SNPshotrs142609245
SNPdbers142609245
MSV3drs142609245
GWAS Ctlgrs142609245
Max Magnitude0
ClinVar
Risk rs142609245(C;C)
Alt rs142609245(C;C)
Reference rs142609245(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFB3
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.201943669T>C
CLNSRC
CLNACC RCV000239318.1,