rs193922275

Orientation

minus

Stabilized

minus

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

Make rs193922275(-;-)

Make rs193922275(-;GC)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44145250

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs193922275
dbSNP (classic)	rs193922275
ClinGen	rs193922275
ebi	rs193922275
HLI	rs193922275
Exac	rs193922275
Gnomad	rs193922275
Varsome	rs193922275
LitVar	rs193922275
Map	rs193922275
PheGenI	rs193922275
Biobank	rs193922275
1000 genomes	rs193922275
hgdp	rs193922275
ensembl	rs193922275
geneview	rs193922275
scholar	rs193922275
google	rs193922275
pharmgkb	rs193922275
gwascentral	rs193922275
openSNP	rs193922275
23andMe	rs193922275
SNPshot	rs193922275
SNPdbe	rs193922275
MSV3d	rs193922275
GWAS Ctlg	rs193922275

Max Magnitude

0

ClinVar
Risk	rs193922275(-;-)
Alt	rs193922275(-;-)
Reference	Rs193922275(GC;GC)
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.44184849_44184850delGC
CLNSRC	ClinVar LabCorp
CLNACC	RCV000029854.1,