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rs515726181

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs515726181(A;A)
Make rs515726181(A;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position102232232
GeneRRM2B
is asnp
is mentioned by
dbSNPrs515726181
ebirs515726181
HLIrs515726181
Exacrs515726181
Varsomers515726181
Maprs515726181
PheGenIrs515726181
hapmaprs515726181
1000 genomesrs515726181
hgdprs515726181
ensemblrs515726181
gopubmedrs515726181
geneviewrs515726181
scholarrs515726181
googlers515726181
pharmgkbrs515726181
gwascentralrs515726181
openSNPrs515726181
23andMers515726181
23andMe allrs515726181
SNP Nexus

SNPshotrs515726181
SNPdbers515726181
MSV3drs515726181
GWAS Ctlgrs515726181
Max Magnitude0
ClinVar
Risk rs515726181(A;A)
Alt rs515726181(A;A)
Reference rs515726181(G;G)
Significance Pathogenic
Disease RRM2B-related mitochondrial disease
Variation info
Gene RRM2B
CLNDBN RRM2B-related mitochondrial disease
Reversed 0
HGVS NC_000008.10:g.103244460G>A
CLNSRC ClinVar
CLNACC RCV000118983.2,