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rs515726183

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs515726183(C;T)
Make rs515726183(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position102226031
GeneRRM2B
is asnp
is mentioned by
dbSNPrs515726183
ebirs515726183
HLIrs515726183
Exacrs515726183
Varsomers515726183
Maprs515726183
PheGenIrs515726183
hapmaprs515726183
1000 genomesrs515726183
hgdprs515726183
ensemblrs515726183
gopubmedrs515726183
geneviewrs515726183
scholarrs515726183
googlers515726183
pharmgkbrs515726183
gwascentralrs515726183
openSNPrs515726183
23andMers515726183
23andMe allrs515726183
SNP Nexus

SNPshotrs515726183
SNPdbers515726183
MSV3drs515726183
GWAS Ctlgrs515726183
Max Magnitude0
ClinVar
Risk rs515726183(A,T;A,T)
Alt rs515726183(A,T;A,T)
Reference rs515726183(C;C)
Significance Pathogenic
Disease not provided RRM2B-related mitochondrial disease
Variation info
Gene RRM2B
CLNDBN not provided RRM2B-related mitochondrial disease
Reversed 0
HGVS NC_000008.10:g.103238259C>A; NC_000008.10:g.103238259C>T
CLNSRC ClinVar
CLNACC RCV000196901.2, RCV000118987.2,