Have questions? Visit https://www.reddit.com/r/SNPedia

rs193922592

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs193922592(A;G)
Make rs193922592(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position120978769
GeneHNF1A
is asnp
is mentioned by
dbSNPrs193922592
ebirs193922592
HLIrs193922592
Exacrs193922592
Varsomers193922592
Maprs193922592
PheGenIrs193922592
hapmaprs193922592
1000 genomesrs193922592
hgdprs193922592
ensemblrs193922592
gopubmedrs193922592
geneviewrs193922592
scholarrs193922592
googlers193922592
pharmgkbrs193922592
gwascentralrs193922592
openSNPrs193922592
23andMers193922592
23andMe allrs193922592
SNP Nexus

SNPshotrs193922592
SNPdbers193922592
MSV3drs193922592
GWAS Ctlgrs193922592
Max Magnitude0
ClinVar
Risk rs193922592(G;G)
Alt rs193922592(G;G)
Reference rs193922592(A;A)
Significance Probable-Pathogenic
Disease Maturity-onset diabetes of the young
Variation info
Gene HNF1A
CLNDBN Maturity-onset diabetes of the young, type 3
Reversed 0
HGVS NC_000012.11:g.121416572A>G
CLNSRC ClinVar LabCorp
CLNACC RCV000030495.1,