rs878853246

Orientation

minus

Stabilized

minus

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

Make rs878853246(C;T)

Make rs878853246(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

7

Position

44153397

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs878853246
dbSNP (classic)	rs878853246
ClinGen	rs878853246
ebi	rs878853246
HLI	rs878853246
Exac	rs878853246
Gnomad	rs878853246
Varsome	rs878853246
LitVar	rs878853246
Map	rs878853246
PheGenI	rs878853246
Biobank	rs878853246
1000 genomes	rs878853246
hgdp	rs878853246
ensembl	rs878853246
geneview	rs878853246
scholar	rs878853246
google	rs878853246
pharmgkb	rs878853246
gwascentral	rs878853246
openSNP	rs878853246
23andMe	rs878853246
SNPshot	rs878853246
SNPdbe	rs878853246
MSV3d	rs878853246
GWAS Ctlg	rs878853246

Max Magnitude

0

ClinVar
Risk	rs878853246(T;T)
Alt	rs878853246(T;T)
Reference	Rs878853246(C;C)
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.44192996G>A
CLNSRC
CLNACC	RCV000225041.1,