rs28936371

Orientation

minus

Stabilized

minus

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

Make rs28936371(C;T)

Make rs28936371(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

17394334

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs28936371
dbSNP (classic)	rs28936371
ClinGen	rs28936371
ebi	rs28936371
HLI	rs28936371
Exac	rs28936371
Gnomad	rs28936371
Varsome	rs28936371
LitVar	rs28936371
Map	rs28936371
PheGenI	rs28936371
Biobank	rs28936371
1000 genomes	rs28936371
hgdp	rs28936371
ensembl	rs28936371
geneview	rs28936371
scholar	rs28936371
google	rs28936371
pharmgkb	rs28936371
gwascentral	rs28936371
openSNP	rs28936371
23andMe	rs28936371
SNPshot	rs28936371
SNPdbe	rs28936371
MSV3d	rs28936371
GWAS Ctlg	rs28936371

Max Magnitude

0

OMIM	600509
Desc	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1
Variant	0010
Related	also

ClinVar
Risk	rs28936371(T;T)
Alt	rs28936371(T;T)
Reference	Rs28936371(C;C)
Significance	Other
Disease	Persistent hyperinsulinemic hypoglycemia of infancy
Variation	info
Gene	ABCC8
CLNDBN	Persistent hyperinsulinemic hypoglycemia of infancy
Reversed	1
HGVS	NC_000011.9:g.17415881G>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000009664.5,