rs193922286

Orientation

minus

Stabilized

minus

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

Make rs193922286(A;A)

Make rs193922286(A;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44153363

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs193922286
dbSNP (classic)	rs193922286
ClinGen	rs193922286
ebi	rs193922286
HLI	rs193922286
Exac	rs193922286
Gnomad	rs193922286
Varsome	rs193922286
LitVar	rs193922286
Map	rs193922286
PheGenI	rs193922286
Biobank	rs193922286
1000 genomes	rs193922286
hgdp	rs193922286
ensembl	rs193922286
geneview	rs193922286
scholar	rs193922286
google	rs193922286
pharmgkb	rs193922286
gwascentral	rs193922286
openSNP	rs193922286
23andMe	rs193922286
SNPshot	rs193922286
SNPdbe	rs193922286
MSV3d	rs193922286
GWAS Ctlg	rs193922286

Max Magnitude

0

ClinVar
Risk	rs193922286(A;A)
Alt	rs193922286(A;A)
Reference	Rs193922286(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.44192962G>T
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029867.1,