rs771251369

Merged into

rs151344624

Orientation

plus

Stabilized

plus

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

Make rs771251369(-;-)

Make rs771251369(-;AGA)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

17395888

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs771251369
dbSNP (classic)	rs771251369
ClinGen	rs771251369
ebi	rs771251369
HLI	rs771251369
Exac	rs771251369
Gnomad	rs771251369
Varsome	rs771251369
LitVar	rs771251369
Map	rs771251369
PheGenI	rs771251369
Biobank	rs771251369
1000 genomes	rs771251369
hgdp	rs771251369
ensembl	rs771251369
geneview	rs771251369
scholar	rs771251369
google	rs771251369
pharmgkb	rs771251369
gwascentral	rs771251369
openSNP	rs771251369
23andMe	rs771251369
SNPshot	rs771251369
SNPdbe	rs771251369
MSV3d	rs771251369
GWAS Ctlg	rs771251369

Status

Merged into rs151344624

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs771251369(AGA;AGA)
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.17417435_17417437delAGA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000177757.2, RCV000201913.1,