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rs370009373

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs370009373(G;G)
Make rs370009373(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position206133107
GeneNDUFS1
is asnp
is mentioned by
dbSNPrs370009373
ebirs370009373
HLIrs370009373
Exacrs370009373
Varsomers370009373
Maprs370009373
PheGenIrs370009373
hapmaprs370009373
1000 genomesrs370009373
hgdprs370009373
ensemblrs370009373
gopubmedrs370009373
geneviewrs370009373
scholarrs370009373
googlers370009373
pharmgkbrs370009373
gwascentralrs370009373
openSNPrs370009373
23andMers370009373
23andMe allrs370009373
SNP Nexus

SNPshotrs370009373
SNPdbers370009373
MSV3drs370009373
GWAS Ctlgrs370009373
Max Magnitude0
ClinVar
Risk rs370009373(G;G)
Alt rs370009373(G;G)
Reference rs370009373(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene NDUFS1
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.206997831T>G
CLNSRC
CLNACC RCV000197167.2,