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rs140126185

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs140126185(C;C)
Make rs140126185(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position206147553
GeneNDUFS1
is asnp
is mentioned by
dbSNPrs140126185
ebirs140126185
HLIrs140126185
Exacrs140126185
Varsomers140126185
Maprs140126185
PheGenIrs140126185
hapmaprs140126185
1000 genomesrs140126185
hgdprs140126185
ensemblrs140126185
gopubmedrs140126185
geneviewrs140126185
scholarrs140126185
googlers140126185
pharmgkbrs140126185
gwascentralrs140126185
openSNPrs140126185
23andMers140126185
23andMe allrs140126185
SNP Nexus

SNPshotrs140126185
SNPdbers140126185
MSV3drs140126185
GWAS Ctlgrs140126185
Max Magnitude0
ClinVar
Risk rs140126185(C;C)
Alt rs140126185(C;C)
Reference rs140126185(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.207012277T>C
CLNSRC
CLNACC RCV000197215.2,