rs1057517050

Orientation

minus

Stabilized

minus

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

Make rs1057517050(-;-)

Make rs1057517050(-;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

17396915

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs1057517050
dbSNP (classic)	rs1057517050
ClinGen	rs1057517050
ebi	rs1057517050
HLI	rs1057517050
Exac	rs1057517050
Gnomad	rs1057517050
Varsome	rs1057517050
LitVar	rs1057517050
Map	rs1057517050
PheGenI	rs1057517050
Biobank	rs1057517050
1000 genomes	rs1057517050
hgdp	rs1057517050
ensembl	rs1057517050
geneview	rs1057517050
scholar	rs1057517050
google	rs1057517050
pharmgkb	rs1057517050
gwascentral	rs1057517050
openSNP	rs1057517050
23andMe	rs1057517050
SNPshot	rs1057517050
SNPdbe	rs1057517050
MSV3d	rs1057517050
GWAS Ctlg	rs1057517050

Max Magnitude

0

ClinVar
Risk	rs1057517050(-;-)
Alt	rs1057517050(-;-)
Reference	Rs1057517050(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.17418462delC
CLNSRC
CLNACC	RCV000412039.1,