rs1057524901

Orientation

minus

Stabilized

minus

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

Make rs1057524901(-;-)

Make rs1057524901(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

44145190

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs1057524901
dbSNP (classic)	rs1057524901
ClinGen	rs1057524901
ebi	rs1057524901
HLI	rs1057524901
Exac	rs1057524901
Gnomad	rs1057524901
Varsome	rs1057524901
LitVar	rs1057524901
Map	rs1057524901
PheGenI	rs1057524901
Biobank	rs1057524901
1000 genomes	rs1057524901
hgdp	rs1057524901
ensembl	rs1057524901
geneview	rs1057524901
scholar	rs1057524901
google	rs1057524901
pharmgkb	rs1057524901
gwascentral	rs1057524901
openSNP	rs1057524901
23andMe	rs1057524901
SNPshot	rs1057524901
SNPdbe	rs1057524901
MSV3d	rs1057524901
GWAS Ctlg	rs1057524901

Max Magnitude

0

ClinVar
Risk	rs1057524901(-;-)
Alt	rs1057524901(-;-)
Reference	Rs1057524901(C;C)
Significance	Probable-Pathogenic
Disease	Monogenic diabetes
Variation	info
Gene	GCK
CLNDBN	Monogenic diabetes
Reversed	1
HGVS	NC_000007.13:g.44184789delG
CLNSRC
CLNACC	RCV000445487.1,