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rs374491359

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs374491359(C;C)
Make rs374491359(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position53646306
GeneNDUFS4
is asnp
is mentioned by
dbSNPrs374491359
ebirs374491359
HLIrs374491359
Exacrs374491359
Varsomers374491359
Maprs374491359
PheGenIrs374491359
hapmaprs374491359
1000 genomesrs374491359
hgdprs374491359
ensemblrs374491359
gopubmedrs374491359
geneviewrs374491359
scholarrs374491359
googlers374491359
pharmgkbrs374491359
gwascentralrs374491359
openSNPrs374491359
23andMers374491359
23andMe allrs374491359
SNP Nexus

SNPshotrs374491359
SNPdbers374491359
MSV3drs374491359
GWAS Ctlgrs374491359
Max Magnitude0
ClinVar
Risk rs374491359(A,C,T;A,C,T)
Alt rs374491359(A,C,T;A,C,T)
Reference rs374491359(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene NDUFS4
CLNDBN not provided
Reversed 0
HGVS NC_000005.9:g.52942136G>A
CLNSRC
CLNACC RCV000199395.1,