rs1057516317

Orientation

minus

Stabilized

minus

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

Make rs1057516317(-;-)

Make rs1057516317(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

17402737

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs1057516317
dbSNP (classic)	rs1057516317
ClinGen	rs1057516317
ebi	rs1057516317
HLI	rs1057516317
Exac	rs1057516317
Gnomad	rs1057516317
Varsome	rs1057516317
LitVar	rs1057516317
Map	rs1057516317
PheGenI	rs1057516317
Biobank	rs1057516317
1000 genomes	rs1057516317
hgdp	rs1057516317
ensembl	rs1057516317
geneview	rs1057516317
scholar	rs1057516317
google	rs1057516317
pharmgkb	rs1057516317
gwascentral	rs1057516317
openSNP	rs1057516317
23andMe	rs1057516317
SNPshot	rs1057516317
SNPdbe	rs1057516317
MSV3d	rs1057516317
GWAS Ctlg	rs1057516317

Max Magnitude

0

ClinVar
Risk	rs1057516317(-;-)
Alt	rs1057516317(-;-)
Reference	Rs1057516317(G;G)
Significance	Probable-Pathogenic
Disease	Persistent hyperinsulinemic hypoglycemia of infancy
Variation	info
Gene	ABCC8
CLNDBN	Persistent hyperinsulinemic hypoglycemia of infancy
Reversed	1
HGVS	NC_000011.9:g.17424284delC
CLNSRC
CLNACC	RCV000410895.1,