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rs515726182

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs515726182(A;G)
Make rs515726182(G;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position102232163
GeneRRM2B
is asnp
is mentioned by
dbSNPrs515726182
ebirs515726182
HLIrs515726182
Exacrs515726182
Varsomers515726182
Maprs515726182
PheGenIrs515726182
hapmaprs515726182
1000 genomesrs515726182
hgdprs515726182
ensemblrs515726182
gopubmedrs515726182
geneviewrs515726182
scholarrs515726182
googlers515726182
pharmgkbrs515726182
gwascentralrs515726182
openSNPrs515726182
23andMers515726182
23andMe allrs515726182
SNP Nexus

SNPshotrs515726182
SNPdbers515726182
MSV3drs515726182
GWAS Ctlgrs515726182
Max Magnitude0
ClinVar
Risk rs515726182(G;G)
Alt rs515726182(G;G)
Reference rs515726182(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.103244391A>G
CLNSRC ClinVar
CLNACC RCV000118986.2,