rs137852787

Orientation

plus

Stabilized

plus

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

Make rs137852787(A;A)

Make rs137852787(A;G)

Reference

GRCh38 38.1/141

Chromosome

13

Position

27924519

Gene

PDX1

is a	snp
is	mentioned by
dbSNP	rs137852787
dbSNP (classic)	rs137852787
ClinGen	rs137852787
ebi	rs137852787
HLI	rs137852787
Exac	rs137852787
Gnomad	rs137852787
Varsome	rs137852787
LitVar	rs137852787
Map	rs137852787
PheGenI	rs137852787
Biobank	rs137852787
1000 genomes	rs137852787
hgdp	rs137852787
ensembl	rs137852787
geneview	rs137852787
scholar	rs137852787
google	rs137852787
pharmgkb	rs137852787
gwascentral	rs137852787
openSNP	rs137852787
23andMe	rs137852787
SNPshot	rs137852787
SNPdbe	rs137852787
MSV3d	rs137852787
GWAS Ctlg	rs137852787

Max Magnitude

0

OMIM	600733
Desc
Variant	0007
Related	also

ClinVar
Risk	rs137852787(A;A)
Alt	rs137852787(A;A)
Reference	Rs137852787(G;G)
Significance	Non-pathogenic
Disease	Maturity-onset diabetes of the young Monogenic diabetes
Variation	info
Gene	PDX1
CLNDBN	Maturity-onset diabetes of the young, type 4 Monogenic diabetes
Reversed	0
HGVS	NC_000013.10:g.28498656G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009413.4, RCV000445478.1,