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rs193922471

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GG;GG) 0 common in clinvar
Make rs193922471(C;C)
Make rs193922471(C;GG)
ReferenceGRCh38 38.1/141
Chromosome20
Position44407437
GeneHNF4A
is asnp
is mentioned by
dbSNPrs193922471
ebirs193922471
HLIrs193922471
Exacrs193922471
Varsomers193922471
Maprs193922471
PheGenIrs193922471
hapmaprs193922471
1000 genomesrs193922471
hgdprs193922471
ensemblrs193922471
gopubmedrs193922471
geneviewrs193922471
scholarrs193922471
googlers193922471
pharmgkbrs193922471
gwascentralrs193922471
openSNPrs193922471
23andMers193922471
23andMe allrs193922471
SNP Nexus

SNPshotrs193922471
SNPdbers193922471
MSV3drs193922471
GWAS Ctlgrs193922471
Max Magnitude0
ClinVar
Risk rs193922471(C;C)
Alt rs193922471(C;C)
Reference rs193922471(GG;GG)
Significance Probable-Pathogenic
Disease Maturity-onset diabetes of the young
Variation info
Gene MIR3646 HNF4A
CLNDBN Maturity-onset diabetes of the young, type 1
Reversed 0
HGVS NC_000020.10:g.43036077_43036078delGGinsC
CLNSRC ClinVar LabCorp
CLNACC RCV000030018.1,