rs193922327

Orientation

minus

Stabilized

minus

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

Make rs193922327(A;C)

Make rs193922327(C;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44147753

Gene	GCK, LOC105375258

is a	snp
is	mentioned by
dbSNP	rs193922327
dbSNP (classic)	rs193922327
ClinGen	rs193922327
ebi	rs193922327
HLI	rs193922327
Exac	rs193922327
Gnomad	rs193922327
Varsome	rs193922327
LitVar	rs193922327
Map	rs193922327
PheGenI	rs193922327
Biobank	rs193922327
1000 genomes	rs193922327
hgdp	rs193922327
ensembl	rs193922327
geneview	rs193922327
scholar	rs193922327
google	rs193922327
pharmgkb	rs193922327
gwascentral	rs193922327
openSNP	rs193922327
23andMe	rs193922327
SNPshot	rs193922327
SNPdbe	rs193922327
MSV3d	rs193922327
GWAS Ctlg	rs193922327

Max Magnitude

0

ClinVar
Risk	rs193922327(C;C)
Alt	rs193922327(C;C)
Reference	Rs193922327(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.44187352T>G
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029917.1,