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rs137852787

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137852787(A;A)
Make rs137852787(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position27924519
GenePDX1
is asnp
is mentioned by
dbSNPrs137852787
ebirs137852787
HLIrs137852787
Exacrs137852787
Varsomers137852787
Maprs137852787
PheGenIrs137852787
hapmaprs137852787
1000 genomesrs137852787
hgdprs137852787
ensemblrs137852787
gopubmedrs137852787
geneviewrs137852787
scholarrs137852787
googlers137852787
pharmgkbrs137852787
gwascentralrs137852787
openSNPrs137852787
23andMers137852787
23andMe allrs137852787
SNP Nexus

SNPshotrs137852787
SNPdbers137852787
MSV3drs137852787
GWAS Ctlgrs137852787
Max Magnitude0
OMIM600733
Desc
Variant0007
Relatedalso
ClinVar
Risk rs137852787(A;A)
Alt rs137852787(A;A)
Reference rs137852787(G;G)
Significance Pathogenic
Disease Maturity-onset diabetes of the young
Variation info
Gene PDX1
CLNDBN Maturity-onset diabetes of the young, type 4
Reversed 0
HGVS NC_000013.10:g.28498656G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009413.4,