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rs115232898

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs115232898(C;C)
Make rs115232898(C;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position97699474
GeneDPYD
is asnp
is mentioned by
dbSNPrs115232898
ebirs115232898
HLIrs115232898
Exacrs115232898
Varsomers115232898
Maprs115232898
PheGenIrs115232898
hapmaprs115232898
1000 genomesrs115232898
hgdprs115232898
ensemblrs115232898
gopubmedrs115232898
geneviewrs115232898
scholarrs115232898
googlers115232898
pharmgkbrs115232898
gwascentralrs115232898
openSNPrs115232898
23andMers115232898
23andMe allrs115232898
SNP Nexus

SNPshotrs115232898
SNPdbers115232898
MSV3drs115232898
GWAS Ctlgrs115232898
Max Magnitude0
ClinVar
Risk rs115232898(C;C)
Alt rs115232898(C;C)
Reference rs115232898(T;T)
Significance Untested
Disease not provided
Variation info
Gene DPYD
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.98165030T>C
CLNSRC ClinVar
CLNACC RCV000086496.1,