rs104894009

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;G)	2	associated with MODY2; maturity onset of diabetes in the young (type 2)
(G;G)	0	common in clinvar

Make rs104894009(C;C)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44146587

Gene	GCK, LOC105375258

is a	snp
is	mentioned by
dbSNP	rs104894009
dbSNP (classic)	rs104894009
ClinGen	rs104894009
ebi	rs104894009
HLI	rs104894009
Exac	rs104894009
Gnomad	rs104894009
Varsome	rs104894009
LitVar	rs104894009
Map	rs104894009
PheGenI	rs104894009
Biobank	rs104894009
1000 genomes	rs104894009
hgdp	rs104894009
ensembl	rs104894009
geneview	rs104894009
scholar	rs104894009
google	rs104894009
pharmgkb	rs104894009
gwascentral	rs104894009
openSNP	rs104894009
23andMe	rs104894009
SNPshot	rs104894009
SNPdbe	rs104894009
MSV3d	rs104894009
GWAS Ctlg	rs104894009

Max Magnitude

2

OMIM	138079
Desc
Variant	0005
Related	also

ClinVar
Risk	rs104894009(C;C)
Alt	rs104894009(C;C)
Reference	Rs104894009(G;G)
Significance	Pathogenic
Disease	Maturity-onset diabetes of the young
Variation	info
Gene	GCK
CLNDBN	Maturity-onset diabetes of the young, type 2
Reversed	1
HGVS	NC_000007.13:g.44186186C>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000017516.28,