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rs515726196

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs515726196(A;C)
Make rs515726196(C;C)
ReferenceGRCh38 38.1/142
Chromosome8
Position102218827
GeneRRM2B
is asnp
is mentioned by
dbSNPrs515726196
ebirs515726196
HLIrs515726196
Exacrs515726196
Varsomers515726196
Maprs515726196
PheGenIrs515726196
hapmaprs515726196
1000 genomesrs515726196
hgdprs515726196
ensemblrs515726196
gopubmedrs515726196
geneviewrs515726196
scholarrs515726196
googlers515726196
pharmgkbrs515726196
gwascentralrs515726196
openSNPrs515726196
23andMers515726196
23andMe allrs515726196
SNP Nexus

SNPshotrs515726196
SNPdbers515726196
MSV3drs515726196
GWAS Ctlgrs515726196
Max Magnitude0
ClinVar
Risk rs515726196(C;C)
Alt rs515726196(C;C)
Reference rs515726196(A;A)
Significance Pathogenic
Disease RRM2B-related mitochondrial disease not provided
Variation info
Gene RRM2B
CLNDBN RRM2B-related mitochondrial disease not provided
Reversed 0
HGVS NC_000008.10:g.103231055A>C
CLNSRC ClinVar
CLNACC RCV000119006.2, RCV000199478.1,