Have questions? Visit https://www.reddit.com/r/SNPedia

rs515726188

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs515726188(C;T)
Make rs515726188(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position102224949
GeneRRM2B
is asnp
is mentioned by
dbSNPrs515726188
ebirs515726188
HLIrs515726188
Exacrs515726188
Varsomers515726188
Maprs515726188
PheGenIrs515726188
hapmaprs515726188
1000 genomesrs515726188
hgdprs515726188
ensemblrs515726188
gopubmedrs515726188
geneviewrs515726188
scholarrs515726188
googlers515726188
pharmgkbrs515726188
gwascentralrs515726188
openSNPrs515726188
23andMers515726188
23andMe allrs515726188
SNP Nexus

SNPshotrs515726188
SNPdbers515726188
MSV3drs515726188
GWAS Ctlgrs515726188
Max Magnitude0
ClinVar
Risk rs515726188(T;T)
Alt rs515726188(T;T)
Reference rs515726188(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.103237177C>T
CLNSRC ClinVar
CLNACC RCV000118996.2,