rs1057520109

Orientation

minus

Stabilized

minus

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

Make rs1057520109(G;T)

Make rs1057520109(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

44153338

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs1057520109
dbSNP (classic)	rs1057520109
ClinGen	rs1057520109
ebi	rs1057520109
HLI	rs1057520109
Exac	rs1057520109
Gnomad	rs1057520109
Varsome	rs1057520109
LitVar	rs1057520109
Map	rs1057520109
PheGenI	rs1057520109
Biobank	rs1057520109
1000 genomes	rs1057520109
hgdp	rs1057520109
ensembl	rs1057520109
geneview	rs1057520109
scholar	rs1057520109
google	rs1057520109
pharmgkb	rs1057520109
gwascentral	rs1057520109
openSNP	rs1057520109
23andMe	rs1057520109
SNPshot	rs1057520109
SNPdbe	rs1057520109
MSV3d	rs1057520109
GWAS Ctlg	rs1057520109

Max Magnitude

0

ClinVar
Risk	rs1057520109(A;A) rs1057520109(T;T)
Alt	rs1057520109(A;A) rs1057520109(T;T)
Reference	Rs1057520109(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	GCK
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.44192937C>A; NC_000007.13:g.44192937C>T
CLNSRC
CLNACC	RCV000431394.1, RCV000479407.1,