rs1057521092

Orientation

minus

Stabilized

minus

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

Make rs1057521092(A;A)

Make rs1057521092(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

44145651

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs1057521092
dbSNP (classic)	rs1057521092
ClinGen	rs1057521092
ebi	rs1057521092
HLI	rs1057521092
Exac	rs1057521092
Gnomad	rs1057521092
Varsome	rs1057521092
LitVar	rs1057521092
Map	rs1057521092
PheGenI	rs1057521092
Biobank	rs1057521092
1000 genomes	rs1057521092
hgdp	rs1057521092
ensembl	rs1057521092
geneview	rs1057521092
scholar	rs1057521092
google	rs1057521092
pharmgkb	rs1057521092
gwascentral	rs1057521092
openSNP	rs1057521092
23andMe	rs1057521092
SNPshot	rs1057521092
SNPdbe	rs1057521092
MSV3d	rs1057521092
GWAS Ctlg	rs1057521092

Max Magnitude

0

ClinVar
Risk	rs1057521092(A;A)
Alt	rs1057521092(A;A)
Reference	Rs1057521092(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GCK
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.44185250C>T
CLNSRC
CLNACC	RCV000440624.1,