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rs751831616

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs751831616(C;C)
Make rs751831616(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position102218846
GeneRRM2B
is asnp
is mentioned by
dbSNPrs751831616
ebirs751831616
HLIrs751831616
Exacrs751831616
Varsomers751831616
Maprs751831616
PheGenIrs751831616
hapmaprs751831616
1000 genomesrs751831616
hgdprs751831616
ensemblrs751831616
gopubmedrs751831616
geneviewrs751831616
scholarrs751831616
googlers751831616
pharmgkbrs751831616
gwascentralrs751831616
openSNPrs751831616
23andMers751831616
23andMe allrs751831616
SNP Nexus

SNPshotrs751831616
SNPdbers751831616
MSV3drs751831616
GWAS Ctlgrs751831616
Max Magnitude0
ClinVar
Risk rs751831616(C;C)
Alt rs751831616(C;C)
Reference rs751831616(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RRM2B
CLNDBN not provided
Reversed 0
HGVS NC_000008.10:g.103231074T>C
CLNSRC
CLNACC RCV000200061.1,