rs193922313

Orientation

minus

Stabilized

minus

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

Make rs193922313(G;T)

Make rs193922313(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44149809

Gene	GCK, LOC105375258

is a	snp
is	mentioned by
dbSNP	rs193922313
dbSNP (classic)	rs193922313
ClinGen	rs193922313
ebi	rs193922313
HLI	rs193922313
Exac	rs193922313
Gnomad	rs193922313
Varsome	rs193922313
LitVar	rs193922313
Map	rs193922313
PheGenI	rs193922313
Biobank	rs193922313
1000 genomes	rs193922313
hgdp	rs193922313
ensembl	rs193922313
geneview	rs193922313
scholar	rs193922313
google	rs193922313
pharmgkb	rs193922313
gwascentral	rs193922313
openSNP	rs193922313
23andMe	rs193922313
SNPshot	rs193922313
SNPdbe	rs193922313
MSV3d	rs193922313
GWAS Ctlg	rs193922313

Max Magnitude

0

ClinVar
Risk	rs193922313(T;T)
Alt	rs193922313(T;T)
Reference	Rs193922313(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.44189408C>A
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029899.1,