rs80356661

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs80356661(G;T)

Make rs80356661(T;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

27924341

Gene

PDX1

is a	snp
is	mentioned by
dbSNP	rs80356661
dbSNP (classic)	rs80356661
ClinGen	rs80356661
ebi	rs80356661
HLI	rs80356661
Exac	rs80356661
Gnomad	rs80356661
Varsome	rs80356661
LitVar	rs80356661
Map	rs80356661
PheGenI	rs80356661
Biobank	rs80356661
1000 genomes	rs80356661
hgdp	rs80356661
ensembl	rs80356661
geneview	rs80356661
scholar	rs80356661
google	rs80356661
pharmgkb	rs80356661
gwascentral	rs80356661
openSNP	rs80356661
23andMe	rs80356661
SNPshot	rs80356661
SNPdbe	rs80356661
MSV3d	rs80356661
GWAS Ctlg	rs80356661

Max Magnitude

0

OMIM	600733
Desc
Variant	0008
Related	also

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	RCV000020215.4, RCV000023033.4,

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