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rs515726187

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs515726187(A;G)
Make rs515726187(G;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position102224972
GeneRRM2B
is asnp
is mentioned by
dbSNPrs515726187
ebirs515726187
HLIrs515726187
Exacrs515726187
Varsomers515726187
Maprs515726187
PheGenIrs515726187
hapmaprs515726187
1000 genomesrs515726187
hgdprs515726187
ensemblrs515726187
gopubmedrs515726187
geneviewrs515726187
scholarrs515726187
googlers515726187
pharmgkbrs515726187
gwascentralrs515726187
openSNPrs515726187
23andMers515726187
23andMe allrs515726187
SNP Nexus

SNPshotrs515726187
SNPdbers515726187
MSV3drs515726187
GWAS Ctlgrs515726187
Max Magnitude0
ClinVar
Risk rs515726187(G;G)
Alt rs515726187(G;G)
Reference rs515726187(A;A)
Significance Pathogenic
Disease RRM2B-related mitochondrial disease
Variation info
Gene RRM2B
CLNDBN RRM2B-related mitochondrial disease
Reversed 0
HGVS NC_000008.10:g.103237200A>G
CLNSRC ClinVar
CLNACC RCV000118995.2,