rs193922263

Orientation

minus

Stabilized

minus

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

Make rs193922263(C;T)

Make rs193922263(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44145626

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs193922263
dbSNP (classic)	rs193922263
ClinGen	rs193922263
ebi	rs193922263
HLI	rs193922263
Exac	rs193922263
Gnomad	rs193922263
Varsome	rs193922263
LitVar	rs193922263
Map	rs193922263
PheGenI	rs193922263
Biobank	rs193922263
1000 genomes	rs193922263
hgdp	rs193922263
ensembl	rs193922263
geneview	rs193922263
scholar	rs193922263
google	rs193922263
pharmgkb	rs193922263
gwascentral	rs193922263
openSNP	rs193922263
23andMe	rs193922263
SNPshot	rs193922263
SNPdbe	rs193922263
MSV3d	rs193922263
GWAS Ctlg	rs193922263

Max Magnitude

0

ClinVar
Risk	rs193922263(T;T)
Alt	rs193922263(T;T)
Reference	Rs193922263(C;C)
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.44185225G>A
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029838.1,