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rs137853334

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 rs137853334(T;T)
ReferenceGRCh38 38.1/141
Chromosome20
Position44419813
GeneHNF4A
is asnp
is mentioned by
dbSNPrs137853334
ebirs137853334
HLIrs137853334
Exacrs137853334
Varsomers137853334
Maprs137853334
PheGenIrs137853334
hapmaprs137853334
1000 genomesrs137853334
hgdprs137853334
ensemblrs137853334
gopubmedrs137853334
geneviewrs137853334
scholarrs137853334
googlers137853334
pharmgkbrs137853334
gwascentralrs137853334
openSNPrs137853334
23andMers137853334
23andMe allrs137853334
SNP Nexus

SNPshotrs137853334
SNPdbers137853334
MSV3drs137853334
GWAS Ctlgrs137853334
Max Magnitude2
OMIM600281
Desc
Variant0001
Relatedalso
ClinVar
Risk rs137853334(T;T)
Alt rs137853334(T;T)
Reference rs137853334(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.43048453C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009790.4,