rs1057516665

Orientation

minus

Stabilized

minus

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

Make rs1057516665(-;A)

Make rs1057516665(A;A)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

17442746

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs1057516665
dbSNP (classic)	rs1057516665
ClinGen	rs1057516665
ebi	rs1057516665
HLI	rs1057516665
Exac	rs1057516665
Gnomad	rs1057516665
Varsome	rs1057516665
LitVar	rs1057516665
Map	rs1057516665
PheGenI	rs1057516665
Biobank	rs1057516665
1000 genomes	rs1057516665
hgdp	rs1057516665
ensembl	rs1057516665
geneview	rs1057516665
scholar	rs1057516665
google	rs1057516665
pharmgkb	rs1057516665
gwascentral	rs1057516665
openSNP	rs1057516665
23andMe	rs1057516665
SNPshot	rs1057516665
SNPdbe	rs1057516665
MSV3d	rs1057516665
GWAS Ctlg	rs1057516665

Max Magnitude

0

ClinVar
Risk	rs1057516665(A;A)
Alt	rs1057516665(A;A)
Reference	Rs1057516665(-;-)
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.17464293_17464294insT
CLNSRC
CLNACC	RCV000409385.1,