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rs137853336

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 2 associated with MODY1; maturity onset of diabetes in the young (type 1)
Make rs137853336(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position44413714
GeneHNF4A
is asnp
is mentioned by
dbSNPrs137853336
ebirs137853336
HLIrs137853336
Exacrs137853336
Varsomers137853336
Maprs137853336
PheGenIrs137853336
hapmaprs137853336
1000 genomesrs137853336
hgdprs137853336
ensemblrs137853336
gopubmedrs137853336
geneviewrs137853336
scholarrs137853336
googlers137853336
pharmgkbrs137853336
gwascentralrs137853336
openSNPrs137853336
23andMers137853336
23andMe allrs137853336
SNP Nexus

SNPshotrs137853336
SNPdbers137853336
MSV3drs137853336
GWAS Ctlgrs137853336
Max Magnitude2
OMIM600281
Desc
Variant0003
Relatedalso
ClinVar
Risk rs137853336(T;T)
Alt rs137853336(T;T)
Reference rs137853336(C;C)
Significance Pathogenic
Disease Maturity-onset diabetes of the young
Variation info
Gene HNF4A
CLNDBN Maturity-onset diabetes of the young, type 1
Reversed 0
HGVS NC_000020.10:g.43042354C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009792.6,