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rs137853236

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 2 associated with MODY3; maturity onset of diabetes in the young (type 3)
Make rs137853236(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position120997504
GeneHNF1A
is asnp
is mentioned by
dbSNPrs137853236
ebirs137853236
HLIrs137853236
Exacrs137853236
Varsomers137853236
Maprs137853236
PheGenIrs137853236
hapmaprs137853236
1000 genomesrs137853236
hgdprs137853236
ensemblrs137853236
gopubmedrs137853236
geneviewrs137853236
scholarrs137853236
googlers137853236
pharmgkbrs137853236
gwascentralrs137853236
openSNPrs137853236
23andMers137853236
23andMe allrs137853236
SNP Nexus

SNPshotrs137853236
SNPdbers137853236
MSV3drs137853236
GWAS Ctlgrs137853236
Max Magnitude2
OMIM142410
Desc
Variant0002
Relatedalso
ClinVar
Risk rs137853236(T;T)
Alt rs137853236(T;T)
Reference rs137853236(C;C)
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.121435307C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000016065.26,