rs104894016

Orientation

minus

Stabilized

minus

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

Make rs104894016(A;A)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44145618

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs104894016
dbSNP (classic)	rs104894016
ClinGen	rs104894016
ebi	rs104894016
HLI	rs104894016
Exac	rs104894016
Gnomad	rs104894016
Varsome	rs104894016
LitVar	rs104894016
Map	rs104894016
PheGenI	rs104894016
Biobank	rs104894016
1000 genomes	rs104894016
hgdp	rs104894016
ensembl	rs104894016
geneview	rs104894016
scholar	rs104894016
google	rs104894016
pharmgkb	rs104894016
gwascentral	rs104894016
openSNP	rs104894016
23andMe	rs104894016
SNPshot	rs104894016
SNPdbe	rs104894016
MSV3d	rs104894016
GWAS Ctlg	rs104894016

Max Magnitude

2

OMIM	138079
Desc
Variant	0014
Related	also

ClinVar
Risk	rs104894016(A;A)
Alt	rs104894016(A;A)
Reference	Rs104894016(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.44185217C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017527.29,