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rs193922472

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922472(A;G)
Make rs193922472(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position44413735
GeneHNF4A
is asnp
is mentioned by
dbSNPrs193922472
ebirs193922472
HLIrs193922472
Exacrs193922472
Varsomers193922472
Maprs193922472
PheGenIrs193922472
hapmaprs193922472
1000 genomesrs193922472
hgdprs193922472
ensemblrs193922472
gopubmedrs193922472
geneviewrs193922472
scholarrs193922472
googlers193922472
pharmgkbrs193922472
gwascentralrs193922472
openSNPrs193922472
23andMers193922472
23andMe allrs193922472
SNP Nexus

SNPshotrs193922472
SNPdbers193922472
MSV3drs193922472
GWAS Ctlgrs193922472
Max Magnitude0
ClinVar
Risk rs193922472(G;G)
Alt rs193922472(G;G)
Reference rs193922472(A;A)
Significance Probable-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.43042375A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000030019.1,