rs1057524906

Orientation

minus

Stabilized

minus

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

Make rs1057524906(C;C)

Make rs1057524906(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

44153387

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs1057524906
dbSNP (classic)	rs1057524906
ClinGen	rs1057524906
ebi	rs1057524906
HLI	rs1057524906
Exac	rs1057524906
Gnomad	rs1057524906
Varsome	rs1057524906
LitVar	rs1057524906
Map	rs1057524906
PheGenI	rs1057524906
Biobank	rs1057524906
1000 genomes	rs1057524906
hgdp	rs1057524906
ensembl	rs1057524906
geneview	rs1057524906
scholar	rs1057524906
google	rs1057524906
pharmgkb	rs1057524906
gwascentral	rs1057524906
openSNP	rs1057524906
23andMe	rs1057524906
SNPshot	rs1057524906
SNPdbe	rs1057524906
MSV3d	rs1057524906
GWAS Ctlg	rs1057524906

Max Magnitude

0

ClinVar
Risk	rs1057524906(C;C)
Alt	rs1057524906(C;C)
Reference	Rs1057524906(T;T)
Significance	Probable-Pathogenic
Disease	Monogenic diabetes
Variation	info
Gene	GCK
CLNDBN	Monogenic diabetes
Reversed	1
HGVS	NC_000007.13:g.44192986A>G
CLNSRC
CLNACC	RCV000445500.1,