rs1057516404

Orientation

minus

Stabilized

minus

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

Make rs1057516404(A;A)

Make rs1057516404(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

17395230

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs1057516404
dbSNP (classic)	rs1057516404
ClinGen	rs1057516404
ebi	rs1057516404
HLI	rs1057516404
Exac	rs1057516404
Gnomad	rs1057516404
Varsome	rs1057516404
LitVar	rs1057516404
Map	rs1057516404
PheGenI	rs1057516404
Biobank	rs1057516404
1000 genomes	rs1057516404
hgdp	rs1057516404
ensembl	rs1057516404
geneview	rs1057516404
scholar	rs1057516404
google	rs1057516404
pharmgkb	rs1057516404
gwascentral	rs1057516404
openSNP	rs1057516404
23andMe	rs1057516404
SNPshot	rs1057516404
SNPdbe	rs1057516404
MSV3d	rs1057516404
GWAS Ctlg	rs1057516404

Max Magnitude

0

ClinVar
Risk	rs1057516404(A;A)
Alt	rs1057516404(A;A)
Reference	Rs1057516404(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.17416777C>T
CLNSRC
CLNACC	RCV000409836.1,