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rs863224194

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224194(A;G)
Make rs863224194(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position102226036
GeneRRM2B
is asnp
is mentioned by
dbSNPrs863224194
ebirs863224194
HLIrs863224194
Exacrs863224194
Varsomers863224194
Maprs863224194
PheGenIrs863224194
hapmaprs863224194
1000 genomesrs863224194
hgdprs863224194
ensemblrs863224194
gopubmedrs863224194
geneviewrs863224194
scholarrs863224194
googlers863224194
pharmgkbrs863224194
gwascentralrs863224194
openSNPrs863224194
23andMers863224194
23andMe allrs863224194
SNP Nexus

SNPshotrs863224194
SNPdbers863224194
MSV3drs863224194
GWAS Ctlgrs863224194
Max Magnitude0
ClinVar
Risk rs863224194(G;G)
Alt rs863224194(G;G)
Reference rs863224194(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene RRM2B
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.103238264T>C
CLNSRC
CLNACC RCV000200520.2,