rs193922268

Orientation

minus

Stabilized

minus

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

Make rs193922268(C;C)

Make rs193922268(C;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44145593

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs193922268
dbSNP (classic)	rs193922268
ClinGen	rs193922268
ebi	rs193922268
HLI	rs193922268
Exac	rs193922268
Gnomad	rs193922268
Varsome	rs193922268
LitVar	rs193922268
Map	rs193922268
PheGenI	rs193922268
Biobank	rs193922268
1000 genomes	rs193922268
hgdp	rs193922268
ensembl	rs193922268
geneview	rs193922268
scholar	rs193922268
google	rs193922268
pharmgkb	rs193922268
gwascentral	rs193922268
openSNP	rs193922268
23andMe	rs193922268
SNPshot	rs193922268
SNPdbe	rs193922268
MSV3d	rs193922268
GWAS Ctlg	rs193922268

Max Magnitude

0

ClinVar
Risk	rs193922268(C;C)
Alt	rs193922268(C;C)
Reference	Rs193922268(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.44185192A>G
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029843.1,