rs193922312

Orientation

minus

Stabilized

minus

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

Make rs193922312(C;G)

Make rs193922312(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44149824

Gene	GCK, LOC105375258

is a	snp
is	mentioned by
dbSNP	rs193922312
dbSNP (classic)	rs193922312
ClinGen	rs193922312
ebi	rs193922312
HLI	rs193922312
Exac	rs193922312
Gnomad	rs193922312
Varsome	rs193922312
LitVar	rs193922312
Map	rs193922312
PheGenI	rs193922312
Biobank	rs193922312
1000 genomes	rs193922312
hgdp	rs193922312
ensembl	rs193922312
geneview	rs193922312
scholar	rs193922312
google	rs193922312
pharmgkb	rs193922312
gwascentral	rs193922312
openSNP	rs193922312
23andMe	rs193922312
SNPshot	rs193922312
SNPdbe	rs193922312
MSV3d	rs193922312
GWAS Ctlg	rs193922312

Max Magnitude

0

ClinVar
Risk	rs193922312(G;G)
Alt	rs193922312(G;G)
Reference	Rs193922312(C;C)
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.44189423G>C
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029897.1,