rs587780346

Orientation

minus

Stabilized

minus

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

Make rs587780346(A;C)

Make rs587780346(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

44149823

Gene	GCK, LOC105375258

is a	snp
is	mentioned by
dbSNP	rs587780346
dbSNP (classic)	rs587780346
ClinGen	rs587780346
ebi	rs587780346
HLI	rs587780346
Exac	rs587780346
Gnomad	rs587780346
Varsome	rs587780346
LitVar	rs587780346
Map	rs587780346
PheGenI	rs587780346
Biobank	rs587780346
1000 genomes	rs587780346
hgdp	rs587780346
ensembl	rs587780346
geneview	rs587780346
scholar	rs587780346
google	rs587780346
pharmgkb	rs587780346
gwascentral	rs587780346
openSNP	rs587780346
23andMe	rs587780346
SNPshot	rs587780346
SNPdbe	rs587780346
MSV3d	rs587780346
GWAS Ctlg	rs587780346

Max Magnitude

0

ClinVar
Risk	rs587780346(C;C)
Alt	rs587780346(C;C)
Reference	Rs587780346(A;A)
Significance	Probable-Pathogenic
Disease	Diabetes mellitus
Variation	info
Gene	GCK
CLNDBN	Diabetes mellitus, gestational
Reversed	1
HGVS	NC_000007.13:g.44189422T>G
CLNSRC
CLNACC	RCV000117132.1,