rs193922332

Orientation

minus

Stabilized

minus

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

Make rs193922332(C;C)

Make rs193922332(C;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44147701

Gene	GCK, LOC105375258

is a	snp
is	mentioned by
dbSNP	rs193922332
dbSNP (classic)	rs193922332
ClinGen	rs193922332
ebi	rs193922332
HLI	rs193922332
Exac	rs193922332
Gnomad	rs193922332
Varsome	rs193922332
LitVar	rs193922332
Map	rs193922332
PheGenI	rs193922332
Biobank	rs193922332
1000 genomes	rs193922332
hgdp	rs193922332
ensembl	rs193922332
geneview	rs193922332
scholar	rs193922332
google	rs193922332
pharmgkb	rs193922332
gwascentral	rs193922332
openSNP	rs193922332
23andMe	rs193922332
SNPshot	rs193922332
SNPdbe	rs193922332
MSV3d	rs193922332
GWAS Ctlg	rs193922332

Max Magnitude

0

ClinVar
Risk	rs193922332(C;C)
Alt	rs193922332(C;C)
Reference	Rs193922332(T;T)
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.44187300A>G
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029922.1,