rs104894014

Orientation

minus

Stabilized

minus

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

Make rs104894014(C;T)

Make rs104894014(T;T)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44145167

Gene

GCK

is a	snp
is	mentioned by
dbSNP	rs104894014
dbSNP (classic)	rs104894014
ClinGen	rs104894014
ebi	rs104894014
HLI	rs104894014
Exac	rs104894014
Gnomad	rs104894014
Varsome	rs104894014
LitVar	rs104894014
Map	rs104894014
PheGenI	rs104894014
Biobank	rs104894014
1000 genomes	rs104894014
hgdp	rs104894014
ensembl	rs104894014
geneview	rs104894014
scholar	rs104894014
google	rs104894014
pharmgkb	rs104894014
gwascentral	rs104894014
openSNP	rs104894014
23andMe	rs104894014
SNPshot	rs104894014
SNPdbe	rs104894014
MSV3d	rs104894014
GWAS Ctlg	rs104894014

Max Magnitude

0

OMIM	138079
Desc
Variant	0012
Related	also

ClinVar
Risk	rs104894014(T;T)
Alt	rs104894014(T;T)
Reference	Rs104894014(C;C)
Significance	Pathogenic
Disease	Hyperinsulinemic hypoglycemia familial 3
Variation	info
Gene	GCK
CLNDBN	Hyperinsulinemic hypoglycemia familial 3
Reversed	1
HGVS	NC_000007.13:g.44184766G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017525.27,