rs193922265

Orientation

minus

Stabilized

minus

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

Make rs193922265(A;A)

Make rs193922265(A;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44145614

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs193922265
dbSNP (classic)	rs193922265
ClinGen	rs193922265
ebi	rs193922265
HLI	rs193922265
Exac	rs193922265
Gnomad	rs193922265
Varsome	rs193922265
LitVar	rs193922265
Map	rs193922265
PheGenI	rs193922265
Biobank	rs193922265
1000 genomes	rs193922265
hgdp	rs193922265
ensembl	rs193922265
geneview	rs193922265
scholar	rs193922265
google	rs193922265
pharmgkb	rs193922265
gwascentral	rs193922265
openSNP	rs193922265
23andMe	rs193922265
SNPshot	rs193922265
SNPdbe	rs193922265
MSV3d	rs193922265
GWAS Ctlg	rs193922265

Max Magnitude

0

ClinVar
Risk	rs193922265(A;A)
Alt	rs193922265(A;A)
Reference	Rs193922265(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.44185213G>T
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029840.1,