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rs515726200

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs515726200(A;A)
Make rs515726200(A;C)
ReferenceGRCh38 38.1/142
Chromosome8
Position102208237
GeneRRM2B
is asnp
is mentioned by
dbSNPrs515726200
ebirs515726200
HLIrs515726200
Exacrs515726200
Varsomers515726200
Maprs515726200
PheGenIrs515726200
hapmaprs515726200
1000 genomesrs515726200
hgdprs515726200
ensemblrs515726200
gopubmedrs515726200
geneviewrs515726200
scholarrs515726200
googlers515726200
pharmgkbrs515726200
gwascentralrs515726200
openSNPrs515726200
23andMers515726200
23andMe allrs515726200
SNP Nexus

SNPshotrs515726200
SNPdbers515726200
MSV3drs515726200
GWAS Ctlgrs515726200
Max Magnitude0
ClinVar
Risk rs515726200(A;A)
Alt rs515726200(A;A)
Reference rs515726200(C;C)
Significance Pathogenic
Disease RRM2B-related mitochondrial disease
Variation info
Gene RRM2B
CLNDBN RRM2B-related mitochondrial disease
Reversed 0
HGVS NC_000008.10:g.103220465C>A
CLNSRC ClinVar
CLNACC RCV000119014.2,