rs137852671

Orientation

minus

Stabilized

minus

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

Make rs137852671(A;A)

Make rs137852671(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

17394295

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs137852671
dbSNP (classic)	rs137852671
ClinGen	rs137852671
ebi	rs137852671
HLI	rs137852671
Exac	rs137852671
Gnomad	rs137852671
Varsome	rs137852671
LitVar	rs137852671
Map	rs137852671
PheGenI	rs137852671
Biobank	rs137852671
1000 genomes	rs137852671
hgdp	rs137852671
ensembl	rs137852671
geneview	rs137852671
scholar	rs137852671
google	rs137852671
pharmgkb	rs137852671
gwascentral	rs137852671
openSNP	rs137852671
23andMe	rs137852671
SNPshot	rs137852671
SNPdbe	rs137852671
MSV3d	rs137852671
GWAS Ctlg	rs137852671

Max Magnitude

0

OMIM	600509
Desc
Variant	0011
Related	also

ClinVar
Risk	rs137852671(A;A)
Alt	rs137852671(A;A)
Reference	Rs137852671(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	1
HGVS	NC_000011.9:g.17415842C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009665.4, RCV000201911.1,