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rs142204928

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs142204928(A;A)
Make rs142204928(A;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position44414519
GeneHNF4A
is asnp
is mentioned by
dbSNPrs142204928
ebirs142204928
HLIrs142204928
Exacrs142204928
Varsomers142204928
Maprs142204928
PheGenIrs142204928
hapmaprs142204928
1000 genomesrs142204928
hgdprs142204928
ensemblrs142204928
gopubmedrs142204928
geneviewrs142204928
scholarrs142204928
googlers142204928
pharmgkbrs142204928
gwascentralrs142204928
openSNPrs142204928
23andMers142204928
23andMe allrs142204928
SNP Nexus

SNPshotrs142204928
SNPdbers142204928
MSV3drs142204928
GWAS Ctlgrs142204928
GMAF0.001837
Max Magnitude0
ClinVar
Risk rs142204928(A;A)
Alt rs142204928(A;A)
Reference rs142204928(G;G)
Significance Untested
Disease Maturity-onset diabetes of the young not provided
Variation info
Gene HNF4A
CLNDBN Maturity-onset diabetes of the young, type 1 not provided
Reversed 0
HGVS NC_000020.10:g.43043159G>A
CLNSRC ClinVar LabCorp
CLNACC RCV000030023.2, RCV000117239.1,