rs587780343

Orientation

minus

Stabilized

minus

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

Make rs587780343(G;T)

Make rs587780343(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

44145638

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs587780343
dbSNP (classic)	rs587780343
ClinGen	rs587780343
ebi	rs587780343
HLI	rs587780343
Exac	rs587780343
Gnomad	rs587780343
Varsome	rs587780343
LitVar	rs587780343
Map	rs587780343
PheGenI	rs587780343
Biobank	rs587780343
1000 genomes	rs587780343
hgdp	rs587780343
ensembl	rs587780343
geneview	rs587780343
scholar	rs587780343
google	rs587780343
pharmgkb	rs587780343
gwascentral	rs587780343
openSNP	rs587780343
23andMe	rs587780343
SNPshot	rs587780343
SNPdbe	rs587780343
MSV3d	rs587780343
GWAS Ctlg	rs587780343

Max Magnitude

0

ClinVar
Risk	rs587780343(T;T)
Alt	rs587780343(T;T)
Reference	Rs587780343(G;G)
Significance	Probable-Pathogenic
Disease	Diabetes mellitus
Variation	info
Gene	GCK
CLNDBN	Diabetes mellitus, gestational
Reversed	1
HGVS	NC_000007.13:g.44185237C>A
CLNSRC
CLNACC	RCV000117127.1,