rs28936370

Orientation

minus

Stabilized

minus

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

Make rs28936370(C;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

17396980

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs28936370
dbSNP (classic)	rs28936370
ClinGen	rs28936370
ebi	rs28936370
HLI	rs28936370
Exac	rs28936370
Gnomad	rs28936370
Varsome	rs28936370
LitVar	rs28936370
Map	rs28936370
PheGenI	rs28936370
Biobank	rs28936370
1000 genomes	rs28936370
hgdp	rs28936370
ensembl	rs28936370
geneview	rs28936370
scholar	rs28936370
google	rs28936370
pharmgkb	rs28936370
gwascentral	rs28936370
openSNP	rs28936370
23andMe	rs28936370
SNPshot	rs28936370
SNPdbe	rs28936370
MSV3d	rs28936370
GWAS Ctlg	rs28936370

Max Magnitude

0

OMIM	600509
Desc	HYPERINSULINEMIC HYPOGLYCEMIA, FAMILIAL, 1
Variant	0008
Related	also

OMIM	600509
Desc
Variant	0012
Related	also

ClinVar
Risk	rs28936370(A;A) Rs28936370(C;C)
Alt	rs28936370(A;A) Rs28936370(C;C)
Reference	Rs28936370(G;G)
Significance	Pathogenic
Disease	Persistent hyperinsulinemic hypoglycemia of infancy Leucine-induced hypoglycemia
Variation	info
Gene	ABCC8
CLNDBN	Persistent hyperinsulinemic hypoglycemia of infancy Leucine-induced hypoglycemia
Reversed	1
HGVS	NC_000011.9:g.17418527C>G; NC_000011.9:g.17418527C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009662.2, RCV000009666.3,