rs193922330

Orientation

minus

Stabilized

minus

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

Make rs193922330(C;C)

Make rs193922330(C;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44147734

Gene	GCK, LOC105375258

is a	snp
is	mentioned by
dbSNP	rs193922330
dbSNP (classic)	rs193922330
ClinGen	rs193922330
ebi	rs193922330
HLI	rs193922330
Exac	rs193922330
Gnomad	rs193922330
Varsome	rs193922330
LitVar	rs193922330
Map	rs193922330
PheGenI	rs193922330
Biobank	rs193922330
1000 genomes	rs193922330
hgdp	rs193922330
ensembl	rs193922330
geneview	rs193922330
scholar	rs193922330
google	rs193922330
pharmgkb	rs193922330
gwascentral	rs193922330
openSNP	rs193922330
23andMe	rs193922330
SNPshot	rs193922330
SNPdbe	rs193922330
MSV3d	rs193922330
GWAS Ctlg	rs193922330

Max Magnitude

0

ClinVar
Risk	rs193922330(C;C)
Alt	rs193922330(C;C)
Reference	Rs193922330(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.44187333A>G
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029920.1,