rs104894015

Orientation

minus

Stabilized

minus

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

Make rs104894015(A;G)

Make rs104894015(G;G)

Reference

GRCh38 38.1/141

Chromosome

7

Position

44149798

Gene	GCK, LOC105375258

is a	snp
is	mentioned by
dbSNP	rs104894015
dbSNP (classic)	rs104894015
ClinGen	rs104894015
ebi	rs104894015
HLI	rs104894015
Exac	rs104894015
Gnomad	rs104894015
Varsome	rs104894015
LitVar	rs104894015
Map	rs104894015
PheGenI	rs104894015
Biobank	rs104894015
1000 genomes	rs104894015
hgdp	rs104894015
ensembl	rs104894015
geneview	rs104894015
scholar	rs104894015
google	rs104894015
pharmgkb	rs104894015
gwascentral	rs104894015
openSNP	rs104894015
23andMe	rs104894015
SNPshot	rs104894015
SNPdbe	rs104894015
MSV3d	rs104894015
GWAS Ctlg	rs104894015

Max Magnitude

0

OMIM	138079
Desc
Variant	0013
Related	also

ClinVar
Risk	rs104894015(G;G)
Alt	rs104894015(G;G)
Reference	Rs104894015(A;A)
Significance	Pathogenic
Disease	Hyperinsulinemic hypoglycemia familial 3
Variation	info
Gene	GCK
CLNDBN	Hyperinsulinemic hypoglycemia familial 3
Reversed	1
HGVS	NC_000007.13:g.44189397T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000017526.27,