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rs488087

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs488087(C;T)
Make rs488087(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position133071212
GeneCEL
is asnp
is mentioned by
dbSNPrs488087
ebirs488087
HLIrs488087
Exacrs488087
Varsomers488087
Maprs488087
PheGenIrs488087
hapmaprs488087
1000 genomesrs488087
hgdprs488087
ensemblrs488087
gopubmedrs488087
geneviewrs488087
scholarrs488087
googlers488087
pharmgkbrs488087
gwascentralrs488087
openSNPrs488087
23andMers488087
23andMe allrs488087
SNP Nexus

SNPshotrs488087
SNPdbers488087
MSV3drs488087
GWAS Ctlgrs488087
Max Magnitude0

[PMID 26498142] Rs488087 single nucleotide polymorphism as predictive risk factor for pancreatic cancers

ClinVar
Risk rs488087(T;T)
Alt rs488087(T;T)
Reference rs488087(C;C)
Significance Probable-non-pathogenic
Disease not specified
Variation info
Gene CEL
CLNDBN not specified
Reversed 0
HGVS NC_000009.11:g.135946599C>T
CLNSRC
CLNACC RCV000116657.2,