rs193922267

Orientation

minus

Stabilized

minus

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

Make rs193922267(A;A)

Make rs193922267(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44145597

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs193922267
dbSNP (classic)	rs193922267
ClinGen	rs193922267
ebi	rs193922267
HLI	rs193922267
Exac	rs193922267
Gnomad	rs193922267
Varsome	rs193922267
LitVar	rs193922267
Map	rs193922267
PheGenI	rs193922267
Biobank	rs193922267
1000 genomes	rs193922267
hgdp	rs193922267
ensembl	rs193922267
geneview	rs193922267
scholar	rs193922267
google	rs193922267
pharmgkb	rs193922267
gwascentral	rs193922267
openSNP	rs193922267
23andMe	rs193922267
SNPshot	rs193922267
SNPdbe	rs193922267
MSV3d	rs193922267
GWAS Ctlg	rs193922267

Max Magnitude

0

ClinVar
Risk	rs193922267(A;A)
Alt	rs193922267(A;A)
Reference	Rs193922267(G;G)
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.44185196C>T
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029842.1,