rs570388861

Orientation

plus

Stabilized

plus

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

Make rs570388861(A;A)

Make rs570388861(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

17408415

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs570388861
dbSNP (classic)	rs570388861
ClinGen	rs570388861
ebi	rs570388861
HLI	rs570388861
Exac	rs570388861
Gnomad	rs570388861
Varsome	rs570388861
LitVar	rs570388861
Map	rs570388861
PheGenI	rs570388861
Biobank	rs570388861
1000 genomes	rs570388861
hgdp	rs570388861
ensembl	rs570388861
geneview	rs570388861
scholar	rs570388861
google	rs570388861
pharmgkb	rs570388861
gwascentral	rs570388861
openSNP	rs570388861
23andMe	rs570388861
SNPshot	rs570388861
SNPdbe	rs570388861
MSV3d	rs570388861
GWAS Ctlg	rs570388861

Max Magnitude

0

ClinVar
Risk	rs570388861(A;A) rs570388861(C;C)
Alt	rs570388861(A;A) rs570388861(C;C)
Reference	Rs570388861(G;G)
Significance	Pathogenic
Disease	Persistent hyperinsulinemic hypoglycemia of infancy not provided
Variation	info
Gene	ABCC8
CLNDBN	Persistent hyperinsulinemic hypoglycemia of infancy not provided
Reversed	0
HGVS	NC_000011.9:g.17429962G>A
CLNSRC	Counsyl
CLNACC	RCV000169216.1, RCV000201910.1,