rs193922333

Orientation

minus

Stabilized

minus

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

Make rs193922333(A;T)

Make rs193922333(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44147680

Gene	GCK, LOC105375258

is a	snp
is	mentioned by
dbSNP	rs193922333
dbSNP (classic)	rs193922333
ClinGen	rs193922333
ebi	rs193922333
HLI	rs193922333
Exac	rs193922333
Gnomad	rs193922333
Varsome	rs193922333
LitVar	rs193922333
Map	rs193922333
PheGenI	rs193922333
Biobank	rs193922333
1000 genomes	rs193922333
hgdp	rs193922333
ensembl	rs193922333
geneview	rs193922333
scholar	rs193922333
google	rs193922333
pharmgkb	rs193922333
gwascentral	rs193922333
openSNP	rs193922333
23andMe	rs193922333
SNPshot	rs193922333
SNPdbe	rs193922333
MSV3d	rs193922333
GWAS Ctlg	rs193922333

Max Magnitude

0

ClinVar
Risk	rs193922333(T;T)
Alt	rs193922333(T;T)
Reference	Rs193922333(A;A)
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.44187279T>A
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029923.1,