rs193922292

Orientation

minus

Stabilized

minus

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

Make rs193922292(G;G)

Make rs193922292(G;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44152312

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs193922292
dbSNP (classic)	rs193922292
ClinGen	rs193922292
ebi	rs193922292
HLI	rs193922292
Exac	rs193922292
Gnomad	rs193922292
Varsome	rs193922292
LitVar	rs193922292
Map	rs193922292
PheGenI	rs193922292
Biobank	rs193922292
1000 genomes	rs193922292
hgdp	rs193922292
ensembl	rs193922292
geneview	rs193922292
scholar	rs193922292
google	rs193922292
pharmgkb	rs193922292
gwascentral	rs193922292
openSNP	rs193922292
23andMe	rs193922292
SNPshot	rs193922292
SNPdbe	rs193922292
MSV3d	rs193922292
GWAS Ctlg	rs193922292

Max Magnitude

0

ClinVar
Risk	rs193922292(G;G)
Alt	rs193922292(G;G)
Reference	Rs193922292(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.44191911A>C
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029875.1,