rs1799857

Orientation

minus

Stabilized

minus

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

Make rs1799857(C;T)

Make rs1799857(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

17430945

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs1799857
dbSNP (classic)	rs1799857
ClinGen	rs1799857
ebi	rs1799857
HLI	rs1799857
Exac	rs1799857
Gnomad	rs1799857
Varsome	rs1799857
LitVar	rs1799857
Map	rs1799857
PheGenI	rs1799857
Biobank	rs1799857
1000 genomes	rs1799857
hgdp	rs1799857
ensembl	rs1799857
geneview	rs1799857
scholar	rs1799857
google	rs1799857
pharmgkb	rs1799857
gwascentral	rs1799857
openSNP	rs1799857
23andMe	rs1799857
SNPshot	rs1799857
SNPdbe	rs1799857
MSV3d	rs1799857
GWAS Ctlg	rs1799857

Max Magnitude

0

[PMID 27677908] ABCC8 Single Nucleotide Polymorphisms are Associated with Cerebral Edema in Severe TBI.

ClinVar
Risk	rs1799857(A;A) rs1799857(G;G) rs1799857(T;T)
Alt	rs1799857(A;A) rs1799857(G;G) rs1799857(T;T)
Reference	Rs1799857(C;C)
Significance	Other
Disease	not specified Transient Neonatal Diabetes Hyperinsulinism Permanent neonatal diabetes mellitus
Variation	info
Gene	ABCC8
CLNDBN	not specified Transient Neonatal Diabetes, Dominant Hyperinsulinism, Dominant/Recessive Permanent neonatal diabetes mellitus
Reversed	1
HGVS	NC_000011.9:g.17452492G>A
CLNSRC
CLNACC	RCV000144979.2, RCV000302706.1, RCV000359236.1, RCV000402117.1,