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rs587780357

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780357(A;A)
Make rs587780357(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome12
Position120993601
GeneHNF1A
is asnp
is mentioned by
dbSNPrs587780357
ebirs587780357
HLIrs587780357
Exacrs587780357
Varsomers587780357
Maprs587780357
PheGenIrs587780357
hapmaprs587780357
1000 genomesrs587780357
hgdprs587780357
ensemblrs587780357
gopubmedrs587780357
geneviewrs587780357
scholarrs587780357
googlers587780357
pharmgkbrs587780357
gwascentralrs587780357
openSNPrs587780357
23andMers587780357
23andMe allrs587780357
SNP Nexus

SNPshotrs587780357
SNPdbers587780357
MSV3drs587780357
GWAS Ctlgrs587780357
Max Magnitude0
ClinVar
Risk rs587780357(A;A)
Alt rs587780357(A;A)
Reference rs587780357(G;G)
Significance Probable-Pathogenic
Disease Diabetes mellitus type 1
Variation info
Gene HNF1A
CLNDBN Diabetes mellitus type 1
Reversed 0
HGVS NC_000012.11:g.121431404G>A
CLNSRC
CLNACC RCV000117232.1,