rs1057516860

Orientation

minus

Stabilized

minus

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

Make rs1057516860(-;-)

Make rs1057516860(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

17428609

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs1057516860
dbSNP (classic)	rs1057516860
ClinGen	rs1057516860
ebi	rs1057516860
HLI	rs1057516860
Exac	rs1057516860
Gnomad	rs1057516860
Varsome	rs1057516860
LitVar	rs1057516860
Map	rs1057516860
PheGenI	rs1057516860
Biobank	rs1057516860
1000 genomes	rs1057516860
hgdp	rs1057516860
ensembl	rs1057516860
geneview	rs1057516860
scholar	rs1057516860
google	rs1057516860
pharmgkb	rs1057516860
gwascentral	rs1057516860
openSNP	rs1057516860
23andMe	rs1057516860
SNPshot	rs1057516860
SNPdbe	rs1057516860
MSV3d	rs1057516860
GWAS Ctlg	rs1057516860

Max Magnitude

0

ClinVar
Risk	rs1057516860(-;-)
Alt	rs1057516860(-;-)
Reference	Rs1057516860(C;C)
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.17450156delG
CLNSRC
CLNACC	RCV000409962.1,