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rs376722149

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs376722149(C;T)
Make rs376722149(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position47584422
GeneNDUFS3
is asnp
is mentioned by
dbSNPrs376722149
ebirs376722149
HLIrs376722149
Exacrs376722149
Varsomers376722149
Maprs376722149
PheGenIrs376722149
hapmaprs376722149
1000 genomesrs376722149
hgdprs376722149
ensemblrs376722149
gopubmedrs376722149
geneviewrs376722149
scholarrs376722149
googlers376722149
pharmgkbrs376722149
gwascentralrs376722149
openSNPrs376722149
23andMers376722149
23andMe allrs376722149
SNP Nexus

SNPshotrs376722149
SNPdbers376722149
MSV3drs376722149
GWAS Ctlgrs376722149
Max Magnitude0
ClinVar
Risk rs376722149(T;T)
Alt rs376722149(T;T)
Reference rs376722149(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFS3
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.47605974C>T
CLNSRC
CLNACC RCV000198333.2,