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rs863224192

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224192(A;A)
Make rs863224192(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position102218899
GeneRRM2B
is asnp
is mentioned by
dbSNPrs863224192
ebirs863224192
HLIrs863224192
Exacrs863224192
Varsomers863224192
Maprs863224192
PheGenIrs863224192
hapmaprs863224192
1000 genomesrs863224192
hgdprs863224192
ensemblrs863224192
gopubmedrs863224192
geneviewrs863224192
scholarrs863224192
googlers863224192
pharmgkbrs863224192
gwascentralrs863224192
openSNPrs863224192
23andMers863224192
23andMe allrs863224192
SNP Nexus

SNPshotrs863224192
SNPdbers863224192
MSV3drs863224192
GWAS Ctlgrs863224192
Max Magnitude0
ClinVar
Risk rs863224192(A;A)
Alt rs863224192(A;A)
Reference rs863224192(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene RRM2B
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.103231127C>T
CLNSRC
CLNACC RCV000196346.1,