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rs137852786

From SNPedia

Orientationplus
Stabilizedplus
Make rs137852786(A;A)
Make rs137852786(A;G)
Make rs137852786(G;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position27924439
GenePDX1
is asnp
is mentioned by
dbSNPrs137852786
dbSNP (old)rs137852786
ClinGenrs137852786
ebirs137852786
HLIrs137852786
Exacrs137852786
Varsomers137852786
Maprs137852786
PheGenIrs137852786
Biobankrs137852786
1000 genomesrs137852786
hgdprs137852786
ensemblrs137852786
gopubmedrs137852786
geneviewrs137852786
scholarrs137852786
googlers137852786
pharmgkbrs137852786
gwascentralrs137852786
openSNPrs137852786
23andMers137852786
23andMe allrs137852786
SNP Nexus

SNPshotrs137852786
SNPdbers137852786
MSV3drs137852786
GWAS Ctlgrs137852786
Max Magnitude
OMIM600733
Desc
Variant0006
Relatedalso
ClinVar
Risk rs137852786(A;A)
Alt rs137852786(A;A)
Reference rs137852786(G;G)
Significance Other
Disease DIABETES MELLITUS
Variation info
Gene PDX1
CLNDBN DIABETES MELLITUS, TYPE II, SUSCEPTIBILITY TO
Reversed 0
HGVS NC_000013.10:g.28498576G>A
CLNSRC OMIM Allelic Variant UniProtKB (protein)
CLNACC RCV000009408.4,