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rs863224193

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224193(A;G)
Make rs863224193(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position102218836
GeneRRM2B
is asnp
is mentioned by
dbSNPrs863224193
ebirs863224193
HLIrs863224193
Exacrs863224193
Varsomers863224193
Maprs863224193
PheGenIrs863224193
hapmaprs863224193
1000 genomesrs863224193
hgdprs863224193
ensemblrs863224193
gopubmedrs863224193
geneviewrs863224193
scholarrs863224193
googlers863224193
pharmgkbrs863224193
gwascentralrs863224193
openSNPrs863224193
23andMers863224193
23andMe allrs863224193
SNP Nexus

SNPshotrs863224193
SNPdbers863224193
MSV3drs863224193
GWAS Ctlgrs863224193
Max Magnitude0
ClinVar
Risk rs863224193(G;G)
Alt rs863224193(G;G)
Reference rs863224193(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene RRM2B
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.103231064T>C
CLNSRC
CLNACC RCV000196496.2,