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rs515726195

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs515726195(C;T)
Make rs515726195(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position102218866
GeneRRM2B
is asnp
is mentioned by
dbSNPrs515726195
ebirs515726195
HLIrs515726195
Exacrs515726195
Varsomers515726195
Maprs515726195
PheGenIrs515726195
hapmaprs515726195
1000 genomesrs515726195
hgdprs515726195
ensemblrs515726195
gopubmedrs515726195
geneviewrs515726195
scholarrs515726195
googlers515726195
pharmgkbrs515726195
gwascentralrs515726195
openSNPrs515726195
23andMers515726195
23andMe allrs515726195
SNP Nexus

SNPshotrs515726195
SNPdbers515726195
MSV3drs515726195
GWAS Ctlgrs515726195
Max Magnitude0
ClinVar
Risk rs515726195(T;T)
Alt rs515726195(T;T)
Reference rs515726195(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.103231094C>T
CLNSRC ClinVar
CLNACC RCV000119004.2,