rs193922303

Orientation

minus

Stabilized

minus

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

Make rs193922303(G;T)

Make rs193922303(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44150039

Gene	GCK, LOC105375258

is a	snp
is	mentioned by
dbSNP	rs193922303
dbSNP (classic)	rs193922303
ClinGen	rs193922303
ebi	rs193922303
HLI	rs193922303
Exac	rs193922303
Gnomad	rs193922303
Varsome	rs193922303
LitVar	rs193922303
Map	rs193922303
PheGenI	rs193922303
Biobank	rs193922303
1000 genomes	rs193922303
hgdp	rs193922303
ensembl	rs193922303
geneview	rs193922303
scholar	rs193922303
google	rs193922303
pharmgkb	rs193922303
gwascentral	rs193922303
openSNP	rs193922303
23andMe	rs193922303
SNPshot	rs193922303
SNPdbe	rs193922303
MSV3d	rs193922303
GWAS Ctlg	rs193922303

Max Magnitude

0

ClinVar
Risk	rs193922303(T;T)
Alt	rs193922303(T;T)
Reference	Rs193922303(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.44189638C>A
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029888.1,