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rs80356661

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs80356661(G;T)
Make rs80356661(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position27924341
GenePDX1
is asnp
is mentioned by
dbSNPrs80356661
ebirs80356661
HLIrs80356661
Exacrs80356661
Varsomers80356661
Maprs80356661
PheGenIrs80356661
hapmaprs80356661
1000 genomesrs80356661
hgdprs80356661
ensemblrs80356661
gopubmedrs80356661
geneviewrs80356661
scholarrs80356661
googlers80356661
pharmgkbrs80356661
gwascentralrs80356661
openSNPrs80356661
23andMers80356661
23andMe allrs80356661
SNP Nexus

SNPshotrs80356661
SNPdbers80356661
MSV3drs80356661
GWAS Ctlgrs80356661
Max Magnitude0
OMIM600733
Desc
Variant0008
Relatedalso
ClinVar
Risk rs80356661(T;T)
Alt rs80356661(T;T)
Reference rs80356661(G;G)
Significance Other
Disease Pancreatic agenesis DIABETES MELLITUS
Variation info
Gene PDX1
CLNDBN Pancreatic agenesis, congenital DIABETES MELLITUS, TYPE II, SUSCEPTIBILITY TO
Reversed 0
HGVS NC_000013.10:g.28498478G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000020215.3, RCV000023033.3,


[PMID 12970316] Agenesis of human pancreas due to decreased half-life of insulin promoter factor 1.