rs1057521093

Orientation

minus

Stabilized

minus

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

Make rs1057521093(A;G)

Make rs1057521093(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

44147810

Gene	GCK, LOC105375258

is a	snp
is	mentioned by
dbSNP	rs1057521093
dbSNP (classic)	rs1057521093
ClinGen	rs1057521093
ebi	rs1057521093
HLI	rs1057521093
Exac	rs1057521093
Gnomad	rs1057521093
Varsome	rs1057521093
LitVar	rs1057521093
Map	rs1057521093
PheGenI	rs1057521093
Biobank	rs1057521093
1000 genomes	rs1057521093
hgdp	rs1057521093
ensembl	rs1057521093
geneview	rs1057521093
scholar	rs1057521093
google	rs1057521093
pharmgkb	rs1057521093
gwascentral	rs1057521093
openSNP	rs1057521093
23andMe	rs1057521093
SNPshot	rs1057521093
SNPdbe	rs1057521093
MSV3d	rs1057521093
GWAS Ctlg	rs1057521093

Max Magnitude

0

ClinVar
Risk	rs1057521093(G;G)
Alt	rs1057521093(G;G)
Reference	Rs1057521093(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GCK
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.44187409T>C
CLNSRC
CLNACC	RCV000419860.1,