rs193922304

Orientation

minus

Stabilized

minus

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

Make rs193922304(C;G)

Make rs193922304(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44150021

Gene	GCK, LOC105375258

is a	snp
is	mentioned by
dbSNP	rs193922304
dbSNP (classic)	rs193922304
ClinGen	rs193922304
ebi	rs193922304
HLI	rs193922304
Exac	rs193922304
Gnomad	rs193922304
Varsome	rs193922304
LitVar	rs193922304
Map	rs193922304
PheGenI	rs193922304
Biobank	rs193922304
1000 genomes	rs193922304
hgdp	rs193922304
ensembl	rs193922304
geneview	rs193922304
scholar	rs193922304
google	rs193922304
pharmgkb	rs193922304
gwascentral	rs193922304
openSNP	rs193922304
23andMe	rs193922304
SNPshot	rs193922304
SNPdbe	rs193922304
MSV3d	rs193922304
GWAS Ctlg	rs193922304

Max Magnitude

0

ClinVar
Risk	rs193922304(G;G)
Alt	rs193922304(G;G)
Reference	Rs193922304(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.44189620G>C
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029889.1,