rs193922259

Orientation

minus

Stabilized

minus

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

Make rs193922259(A;T)

Make rs193922259(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44153406

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs193922259
dbSNP (classic)	rs193922259
ClinGen	rs193922259
ebi	rs193922259
HLI	rs193922259
Exac	rs193922259
Gnomad	rs193922259
Varsome	rs193922259
LitVar	rs193922259
Map	rs193922259
PheGenI	rs193922259
Biobank	rs193922259
1000 genomes	rs193922259
hgdp	rs193922259
ensembl	rs193922259
geneview	rs193922259
scholar	rs193922259
google	rs193922259
pharmgkb	rs193922259
gwascentral	rs193922259
openSNP	rs193922259
23andMe	rs193922259
SNPshot	rs193922259
SNPdbe	rs193922259
MSV3d	rs193922259
GWAS Ctlg	rs193922259

Max Magnitude

0

ClinVar
Risk	rs193922259(T;T)
Alt	rs193922259(T;T)
Reference	Rs193922259(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.44193005T>A
CLNSRC	ClinVar
CLNACC	RCV000029834.1,