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rs137853237

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 2 associated with MODY3; maturity onset of diabetes in the young (type 3)
Make rs137853237(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position120988871
GeneHNF1A
is asnp
is mentioned by
dbSNPrs137853237
ebirs137853237
HLIrs137853237
Exacrs137853237
Varsomers137853237
Maprs137853237
PheGenIrs137853237
hapmaprs137853237
1000 genomesrs137853237
hgdprs137853237
ensemblrs137853237
gopubmedrs137853237
geneviewrs137853237
scholarrs137853237
googlers137853237
pharmgkbrs137853237
gwascentralrs137853237
openSNPrs137853237
23andMers137853237
23andMe allrs137853237
SNP Nexus

SNPshotrs137853237
SNPdbers137853237
MSV3drs137853237
GWAS Ctlgrs137853237
Max Magnitude2
OMIM142410
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137853237(G;G)
Alt rs137853237(G;G)
Reference rs137853237(A;A)
Significance Pathogenic
Disease Maturity-onset diabetes of the young
Variation info
Gene HNF1A
CLNDBN Maturity-onset diabetes of the young, type 3
Reversed 0
HGVS NC_000012.11:g.121426674A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000016067.22,