rs1057517128

Orientation

minus

Stabilized

minus

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

Make rs1057517128(C;C)

Make rs1057517128(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

17443176

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs1057517128
dbSNP (classic)	rs1057517128
ClinGen	rs1057517128
ebi	rs1057517128
HLI	rs1057517128
Exac	rs1057517128
Gnomad	rs1057517128
Varsome	rs1057517128
LitVar	rs1057517128
Map	rs1057517128
PheGenI	rs1057517128
Biobank	rs1057517128
1000 genomes	rs1057517128
hgdp	rs1057517128
ensembl	rs1057517128
geneview	rs1057517128
scholar	rs1057517128
google	rs1057517128
pharmgkb	rs1057517128
gwascentral	rs1057517128
openSNP	rs1057517128
23andMe	rs1057517128
SNPshot	rs1057517128
SNPdbe	rs1057517128
MSV3d	rs1057517128
GWAS Ctlg	rs1057517128

Max Magnitude

0

ClinVar
Risk	rs1057517128(C;C)
Alt	rs1057517128(C;C)
Reference	Rs1057517128(T;T)
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.17464723A>G
CLNSRC
CLNACC	RCV000412284.1,