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rs137853337

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;G) 2 associated with MODY1; maturity onset of diabetes in the young (type 1)
(G;G) 0 common in clinvar


Make rs137853337(A;A)
ReferenceGRCh38 38.1/141
Chromosome20
Position44428409
GeneHNF4A
is asnp
is mentioned by
dbSNPrs137853337
ebirs137853337
HLIrs137853337
Exacrs137853337
Varsomers137853337
Maprs137853337
PheGenIrs137853337
hapmaprs137853337
1000 genomesrs137853337
hgdprs137853337
ensemblrs137853337
gopubmedrs137853337
geneviewrs137853337
scholarrs137853337
googlers137853337
pharmgkbrs137853337
gwascentralrs137853337
openSNPrs137853337
23andMers137853337
23andMe allrs137853337
SNP Nexus

SNPshotrs137853337
SNPdbers137853337
MSV3drs137853337
GWAS Ctlgrs137853337
Max Magnitude2
OMIM600281
Desc
Variant0004
Relatedalso
ClinVar
Risk rs137853337(A;A)
Alt rs137853337(A;A)
Reference rs137853337(G;G)
Significance Pathogenic
Disease Diabetes mellitus type 2
Variation info
Gene HNF4A
CLNDBN Diabetes mellitus type 2
Reversed 0
HGVS NC_000020.10:g.43057049G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000009793.6,