rs193922594

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;G)	3.6	Mature onset diabetes of the young (type 3)

Make rs193922594(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

120979081

Gene

HNF1A

is a	snp
is	mentioned by
dbSNP	rs193922594
dbSNP (classic)	rs193922594
ClinGen	rs193922594
ebi	rs193922594
HLI	rs193922594
Exac	rs193922594
Gnomad	rs193922594
Varsome	rs193922594
LitVar	rs193922594
Map	rs193922594
PheGenI	rs193922594
Biobank	rs193922594
1000 genomes	rs193922594
hgdp	rs193922594
ensembl	rs193922594
geneview	rs193922594
scholar	rs193922594
google	rs193922594
pharmgkb	rs193922594
gwascentral	rs193922594
openSNP	rs193922594
23andMe	rs193922594
SNPshot	rs193922594
SNPdbe	rs193922594
MSV3d	rs193922594
GWAS Ctlg	rs193922594

Max Magnitude

3.6

ClinVar
Risk	rs193922594(G;G)
Alt	rs193922594(G;G)
Reference	Rs193922594(-;-)
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.121416884dupG
CLNSRC	ClinVar LabCorp
CLNACC	RCV000030498.1,