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rs863224191

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224191(C;T)
Make rs863224191(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position102224076
GeneRRM2B
is asnp
is mentioned by
dbSNPrs863224191
ebirs863224191
HLIrs863224191
Exacrs863224191
Varsomers863224191
Maprs863224191
PheGenIrs863224191
hapmaprs863224191
1000 genomesrs863224191
hgdprs863224191
ensemblrs863224191
gopubmedrs863224191
geneviewrs863224191
scholarrs863224191
googlers863224191
pharmgkbrs863224191
gwascentralrs863224191
openSNPrs863224191
23andMers863224191
23andMe allrs863224191
SNP Nexus

SNPshotrs863224191
SNPdbers863224191
MSV3drs863224191
GWAS Ctlgrs863224191
Max Magnitude0
ClinVar
Risk rs863224191(T;T)
Alt rs863224191(T;T)
Reference rs863224191(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene RRM2B
CLNDBN not provided
Reversed 1
HGVS NC_000008.10:g.103236304G>A
CLNSRC
CLNACC RCV000199844.1,