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

rs182614164

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs182614164(C;G)
Make rs182614164(G;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position102212833
GeneRRM2B
is asnp
is mentioned by
dbSNPrs182614164
ebirs182614164
HLIrs182614164
Exacrs182614164
Varsomers182614164
Maprs182614164
PheGenIrs182614164
hapmaprs182614164
1000 genomesrs182614164
hgdprs182614164
ensemblrs182614164
gopubmedrs182614164
geneviewrs182614164
scholarrs182614164
googlers182614164
pharmgkbrs182614164
gwascentralrs182614164
openSNPrs182614164
23andMers182614164
23andMe allrs182614164
SNP Nexus

SNPshotrs182614164
SNPdbers182614164
MSV3drs182614164
GWAS Ctlgrs182614164
Max Magnitude0
ClinVar
Risk rs182614164(G;G)
Alt rs182614164(G;G)
Reference rs182614164(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.103225061C>G
CLNSRC ClinVar
CLNACC RCV000119009.2,