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rs515726198

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs515726198(A;C)
Make rs515726198(C;C)
ReferenceGRCh38 38.1/142
Chromosome8
Position102208240
GeneRRM2B
is asnp
is mentioned by
dbSNPrs515726198
ebirs515726198
HLIrs515726198
Exacrs515726198
Varsomers515726198
Maprs515726198
PheGenIrs515726198
hapmaprs515726198
1000 genomesrs515726198
hgdprs515726198
ensemblrs515726198
gopubmedrs515726198
geneviewrs515726198
scholarrs515726198
googlers515726198
pharmgkbrs515726198
gwascentralrs515726198
openSNPrs515726198
23andMers515726198
23andMe allrs515726198
SNP Nexus

SNPshotrs515726198
SNPdbers515726198
MSV3drs515726198
GWAS Ctlgrs515726198
Max Magnitude0
ClinVar
Risk rs515726198(C;C)
Alt rs515726198(C;C)
Reference rs515726198(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.103220468A>C
CLNSRC ClinVar
CLNACC RCV000119012.2,