rs193922290

Orientation

minus

Stabilized

minus

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

Make rs193922290(A;T)

Make rs193922290(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44152381

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs193922290
dbSNP (classic)	rs193922290
ClinGen	rs193922290
ebi	rs193922290
HLI	rs193922290
Exac	rs193922290
Gnomad	rs193922290
Varsome	rs193922290
LitVar	rs193922290
Map	rs193922290
PheGenI	rs193922290
Biobank	rs193922290
1000 genomes	rs193922290
hgdp	rs193922290
ensembl	rs193922290
geneview	rs193922290
scholar	rs193922290
google	rs193922290
pharmgkb	rs193922290
gwascentral	rs193922290
openSNP	rs193922290
23andMe	rs193922290
SNPshot	rs193922290
SNPdbe	rs193922290
MSV3d	rs193922290
GWAS Ctlg	rs193922290

Max Magnitude

0

ClinVar
Risk	rs193922290(T;T)
Alt	rs193922290(T;T)
Reference	Rs193922290(A;A)
Significance	Probable-Pathogenic
Disease	Maturity-onset diabetes of the young
Variation	info
Gene	GCK
CLNDBN	Maturity-onset diabetes of the young, type 2
Reversed	1
HGVS	NC_000007.13:g.44191980T>A
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029873.1,