rs587780345

Orientation

minus

Stabilized

minus

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

Make rs587780345(A;A)

Make rs587780345(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

44150004

Gene	GCK, LOC105375258

is a	snp
is	mentioned by
dbSNP	rs587780345
dbSNP (classic)	rs587780345
ClinGen	rs587780345
ebi	rs587780345
HLI	rs587780345
Exac	rs587780345
Gnomad	rs587780345
Varsome	rs587780345
LitVar	rs587780345
Map	rs587780345
PheGenI	rs587780345
Biobank	rs587780345
1000 genomes	rs587780345
hgdp	rs587780345
ensembl	rs587780345
geneview	rs587780345
scholar	rs587780345
google	rs587780345
pharmgkb	rs587780345
gwascentral	rs587780345
openSNP	rs587780345
23andMe	rs587780345
SNPshot	rs587780345
SNPdbe	rs587780345
MSV3d	rs587780345
GWAS Ctlg	rs587780345

Max Magnitude

0

ClinVar
Risk	rs587780345(A;A)
Alt	rs587780345(A;A)
Reference	Rs587780345(G;G)
Significance	Pathogenic
Disease	Diabetes mellitus not provided Maturity-onset diabetes of the young Diabetes mellitus type 2
Variation	info
Gene	GCK
CLNDBN	Diabetes mellitus, gestational not provided Maturity-onset diabetes of the young, type 2 Diabetes mellitus type 2
Reversed	1
HGVS	NC_000007.13:g.44189603C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000117131.1, RCV000255191.1, RCV000271136.1, RCV000328419.1,