rs1057516509

Orientation

minus

Stabilized

minus

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

Make rs1057516509(C;C)

Make rs1057516509(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

17432203

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs1057516509
dbSNP (classic)	rs1057516509
ClinGen	rs1057516509
ebi	rs1057516509
HLI	rs1057516509
Exac	rs1057516509
Gnomad	rs1057516509
Varsome	rs1057516509
LitVar	rs1057516509
Map	rs1057516509
PheGenI	rs1057516509
Biobank	rs1057516509
1000 genomes	rs1057516509
hgdp	rs1057516509
ensembl	rs1057516509
geneview	rs1057516509
scholar	rs1057516509
google	rs1057516509
pharmgkb	rs1057516509
gwascentral	rs1057516509
openSNP	rs1057516509
23andMe	rs1057516509
SNPshot	rs1057516509
SNPdbe	rs1057516509
MSV3d	rs1057516509
GWAS Ctlg	rs1057516509

Max Magnitude

0

ClinVar
Risk	rs1057516509(C;C)
Alt	rs1057516509(C;C)
Reference	Rs1057516509(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.17453750C>G
CLNSRC
CLNACC	RCV000412268.1,