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rs137853244

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 rs137853244(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position120988897
GeneHNF1A
is asnp
is mentioned by
dbSNPrs137853244
ebirs137853244
HLIrs137853244
Exacrs137853244
Varsomers137853244
Maprs137853244
PheGenIrs137853244
hapmaprs137853244
1000 genomesrs137853244
hgdprs137853244
ensemblrs137853244
gopubmedrs137853244
geneviewrs137853244
scholarrs137853244
googlers137853244
pharmgkbrs137853244
gwascentralrs137853244
openSNPrs137853244
23andMers137853244
23andMe allrs137853244
SNP Nexus

SNPshotrs137853244
SNPdbers137853244
MSV3drs137853244
GWAS Ctlgrs137853244
Max Magnitude2
OMIM142410
Desc
Variant0016
Relatedalso
ClinVar
Risk rs137853244(T;T)
Alt rs137853244(T;T)
Reference rs137853244(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.121426700C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000016081.22,