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rs515726189

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs515726189(A;A)
Make rs515726189(A;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position102224909
GeneRRM2B
is asnp
is mentioned by
dbSNPrs515726189
ebirs515726189
HLIrs515726189
Exacrs515726189
Varsomers515726189
Maprs515726189
PheGenIrs515726189
hapmaprs515726189
1000 genomesrs515726189
hgdprs515726189
ensemblrs515726189
gopubmedrs515726189
geneviewrs515726189
scholarrs515726189
googlers515726189
pharmgkbrs515726189
gwascentralrs515726189
openSNPrs515726189
23andMers515726189
23andMe allrs515726189
SNP Nexus

SNPshotrs515726189
SNPdbers515726189
MSV3drs515726189
GWAS Ctlgrs515726189
Max Magnitude0
ClinVar
Risk rs515726189(A;A)
Alt rs515726189(A;A)
Reference rs515726189(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.103237137G>A
CLNSRC ClinVar
CLNACC RCV000118997.2,