rs1057517015

Orientation

minus

Stabilized

minus

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

Make rs1057517015(A;G)

Make rs1057517015(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

17463606

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs1057517015
dbSNP (classic)	rs1057517015
ClinGen	rs1057517015
ebi	rs1057517015
HLI	rs1057517015
Exac	rs1057517015
Gnomad	rs1057517015
Varsome	rs1057517015
LitVar	rs1057517015
Map	rs1057517015
PheGenI	rs1057517015
Biobank	rs1057517015
1000 genomes	rs1057517015
hgdp	rs1057517015
ensembl	rs1057517015
geneview	rs1057517015
scholar	rs1057517015
google	rs1057517015
pharmgkb	rs1057517015
gwascentral	rs1057517015
openSNP	rs1057517015
23andMe	rs1057517015
SNPshot	rs1057517015
SNPdbe	rs1057517015
MSV3d	rs1057517015
GWAS Ctlg	rs1057517015

Max Magnitude

0

ClinVar
Risk	rs1057517015(G;G)
Alt	rs1057517015(G;G)
Reference	Rs1057517015(A;A)
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.17485153T>C
CLNSRC
CLNACC	RCV000410546.1,