rs193922592

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs193922592(A;G)

Make rs193922592(G;G)

Reference

GRCh38 38.1/141

Chromosome

12

Position

120978769

Gene

HNF1A

is a	snp
is	mentioned by
dbSNP	rs193922592
dbSNP (classic)	rs193922592
ClinGen	rs193922592
ebi	rs193922592
HLI	rs193922592
Exac	rs193922592
Gnomad	rs193922592
Varsome	rs193922592
LitVar	rs193922592
Map	rs193922592
PheGenI	rs193922592
Biobank	rs193922592
1000 genomes	rs193922592
hgdp	rs193922592
ensembl	rs193922592
geneview	rs193922592
scholar	rs193922592
google	rs193922592
pharmgkb	rs193922592
gwascentral	rs193922592
openSNP	rs193922592
23andMe	rs193922592
SNPshot	rs193922592
SNPdbe	rs193922592
MSV3d	rs193922592
GWAS Ctlg	rs193922592

Max Magnitude

0

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,