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rs515726180

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs515726180(C;T)
Make rs515726180(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position102238827
GeneRRM2B
is asnp
is mentioned by
dbSNPrs515726180
ebirs515726180
HLIrs515726180
Exacrs515726180
Varsomers515726180
Maprs515726180
PheGenIrs515726180
hapmaprs515726180
1000 genomesrs515726180
hgdprs515726180
ensemblrs515726180
gopubmedrs515726180
geneviewrs515726180
scholarrs515726180
googlers515726180
pharmgkbrs515726180
gwascentralrs515726180
openSNPrs515726180
23andMers515726180
23andMe allrs515726180
SNP Nexus

SNPshotrs515726180
SNPdbers515726180
MSV3drs515726180
GWAS Ctlgrs515726180
Max Magnitude0
ClinVar
Risk rs515726180(T;T)
Alt rs515726180(T;T)
Reference rs515726180(C;C)
Significance Pathogenic
Disease RRM2B-related mitochondrial disease
Variation info
Gene RRM2B LOC101927221 UBR5-AS1
CLNDBN RRM2B-related mitochondrial disease
Reversed 0
HGVS NC_000008.10:g.103251055C>T
CLNSRC ClinVar
CLNACC RCV000118982.2,