rs193922322

Orientation

minus

Stabilized

minus

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

Make rs193922322(A;A)

Make rs193922322(A;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44147819

Gene	GCK, LOC105375258

is a	snp
is	mentioned by
dbSNP	rs193922322
dbSNP (classic)	rs193922322
ClinGen	rs193922322
ebi	rs193922322
HLI	rs193922322
Exac	rs193922322
Gnomad	rs193922322
Varsome	rs193922322
LitVar	rs193922322
Map	rs193922322
PheGenI	rs193922322
Biobank	rs193922322
1000 genomes	rs193922322
hgdp	rs193922322
ensembl	rs193922322
geneview	rs193922322
scholar	rs193922322
google	rs193922322
pharmgkb	rs193922322
gwascentral	rs193922322
openSNP	rs193922322
23andMe	rs193922322
SNPshot	rs193922322
SNPdbe	rs193922322
MSV3d	rs193922322
GWAS Ctlg	rs193922322

Max Magnitude

0

ClinVar
Risk	rs193922322(A;A)
Alt	rs193922322(A;A)
Reference	Rs193922322(G;G)
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.44187418C>T
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029910.1,