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rs515726202

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs515726202(C;C)
Make rs515726202(C;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position102208143
GeneRRM2B
is asnp
is mentioned by
dbSNPrs515726202
ebirs515726202
HLIrs515726202
Exacrs515726202
Varsomers515726202
Maprs515726202
PheGenIrs515726202
hapmaprs515726202
1000 genomesrs515726202
hgdprs515726202
ensemblrs515726202
gopubmedrs515726202
geneviewrs515726202
scholarrs515726202
googlers515726202
pharmgkbrs515726202
gwascentralrs515726202
openSNPrs515726202
23andMers515726202
23andMe allrs515726202
SNP Nexus

SNPshotrs515726202
SNPdbers515726202
MSV3drs515726202
GWAS Ctlgrs515726202
Max Magnitude0
ClinVar
Risk rs515726202(C;C)
Alt rs515726202(C;C)
Reference rs515726202(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.103220371G>C
CLNSRC ClinVar
CLNACC RCV000119017.2,