rs1064795242

Orientation

minus

Stabilized

minus

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

Chromosome

7

Position

44145195

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs1064795242
dbSNP (classic)	rs1064795242
ClinGen	rs1064795242
ebi	rs1064795242
HLI	rs1064795242
Exac	rs1064795242
Gnomad	rs1064795242
Varsome	rs1064795242
LitVar	rs1064795242
Map	rs1064795242
PheGenI	rs1064795242
Biobank	rs1064795242
1000 genomes	rs1064795242
hgdp	rs1064795242
ensembl	rs1064795242
geneview	rs1064795242
scholar	rs1064795242
google	rs1064795242
pharmgkb	rs1064795242
gwascentral	rs1064795242
openSNP	rs1064795242
23andMe	rs1064795242
SNPshot	rs1064795242
SNPdbe	rs1064795242
MSV3d	rs1064795242
GWAS Ctlg	rs1064795242

Max Magnitude

0

ClinVar
Risk	rs1064795242(-;-)
Alt	rs1064795242(-;-)
Reference	Rs1064795242(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	GCK
CLNDBN	not provided
Reversed	1
HGVS	NC_000007.13:g.44184794delG
CLNSRC
CLNACC	RCV000481054.1,