rs786204676

Orientation

minus

Stabilized

minus

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

Make rs786204676(C;C)

Make rs786204676(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

17427865

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs786204676
dbSNP (classic)	rs786204676
ClinGen	rs786204676
ebi	rs786204676
HLI	rs786204676
Exac	rs786204676
Gnomad	rs786204676
Varsome	rs786204676
LitVar	rs786204676
Map	rs786204676
PheGenI	rs786204676
Biobank	rs786204676
1000 genomes	rs786204676
hgdp	rs786204676
ensembl	rs786204676
geneview	rs786204676
scholar	rs786204676
google	rs786204676
pharmgkb	rs786204676
gwascentral	rs786204676
openSNP	rs786204676
23andMe	rs786204676
SNPshot	rs786204676
SNPdbe	rs786204676
MSV3d	rs786204676
GWAS Ctlg	rs786204676

Max Magnitude

0

ClinVar
Risk	rs786204676(C;C)
Alt	rs786204676(C;C)
Reference	Rs786204676(T;T)
Significance	Probable-Pathogenic
Disease	Persistent hyperinsulinemic hypoglycemia of infancy
Variation	info
Gene	ABCC8
CLNDBN	Persistent hyperinsulinemic hypoglycemia of infancy
Reversed	1
HGVS	NC_000011.9:g.17449412A>G
CLNSRC	Counsyl
CLNACC	RCV000169482.1,