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rs515726186

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs515726186(A;A)
Make rs515726186(A;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position102225012
GeneRRM2B
is asnp
is mentioned by
dbSNPrs515726186
ebirs515726186
HLIrs515726186
Exacrs515726186
Varsomers515726186
Maprs515726186
PheGenIrs515726186
hapmaprs515726186
1000 genomesrs515726186
hgdprs515726186
ensemblrs515726186
gopubmedrs515726186
geneviewrs515726186
scholarrs515726186
googlers515726186
pharmgkbrs515726186
gwascentralrs515726186
openSNPrs515726186
23andMers515726186
23andMe allrs515726186
SNP Nexus

SNPshotrs515726186
SNPdbers515726186
MSV3drs515726186
GWAS Ctlgrs515726186
Max Magnitude0
ClinVar
Risk rs515726186(A;A)
Alt rs515726186(A;A)
Reference rs515726186(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.103237240G>A
CLNSRC ClinVar
CLNACC RCV000118991.2,