rs193922280

Orientation

minus

Stabilized

minus

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

Make rs193922280(-;-)

Make rs193922280(-;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44145202

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs193922280
dbSNP (classic)	rs193922280
ClinGen	rs193922280
ebi	rs193922280
HLI	rs193922280
Exac	rs193922280
Gnomad	rs193922280
Varsome	rs193922280
LitVar	rs193922280
Map	rs193922280
PheGenI	rs193922280
Biobank	rs193922280
1000 genomes	rs193922280
hgdp	rs193922280
ensembl	rs193922280
geneview	rs193922280
scholar	rs193922280
google	rs193922280
pharmgkb	rs193922280
gwascentral	rs193922280
openSNP	rs193922280
23andMe	rs193922280
SNPshot	rs193922280
SNPdbe	rs193922280
MSV3d	rs193922280
GWAS Ctlg	rs193922280

Max Magnitude

0

ClinVar
Risk	rs193922280(-;-)
Alt	rs193922280(-;-)
Reference	Rs193922280(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.44184801delG
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029860.1,