rs193922269

Orientation

minus

Stabilized

minus

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

Make rs193922269(G;T)

Make rs193922269(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44145575

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs193922269
dbSNP (classic)	rs193922269
ClinGen	rs193922269
ebi	rs193922269
HLI	rs193922269
Exac	rs193922269
Gnomad	rs193922269
Varsome	rs193922269
LitVar	rs193922269
Map	rs193922269
PheGenI	rs193922269
Biobank	rs193922269
1000 genomes	rs193922269
hgdp	rs193922269
ensembl	rs193922269
geneview	rs193922269
scholar	rs193922269
google	rs193922269
pharmgkb	rs193922269
gwascentral	rs193922269
openSNP	rs193922269
23andMe	rs193922269
SNPshot	rs193922269
SNPdbe	rs193922269
MSV3d	rs193922269
GWAS Ctlg	rs193922269

Max Magnitude

0

ClinVar
Risk	rs193922269(T;T)
Alt	rs193922269(T;T)
Reference	Rs193922269(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.44185174C>A
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029848.1,