rs797045207

Orientation

minus

Stabilized

minus

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

Make rs797045207(A;A)

Make rs797045207(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

17427155

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs797045207
dbSNP (classic)	rs797045207
ClinGen	rs797045207
ebi	rs797045207
HLI	rs797045207
Exac	rs797045207
Gnomad	rs797045207
Varsome	rs797045207
LitVar	rs797045207
Map	rs797045207
PheGenI	rs797045207
Biobank	rs797045207
1000 genomes	rs797045207
hgdp	rs797045207
ensembl	rs797045207
geneview	rs797045207
scholar	rs797045207
google	rs797045207
pharmgkb	rs797045207
gwascentral	rs797045207
openSNP	rs797045207
23andMe	rs797045207
SNPshot	rs797045207
SNPdbe	rs797045207
MSV3d	rs797045207
GWAS Ctlg	rs797045207

Max Magnitude

0

ClinVar
Risk	rs797045207(A;A)
Alt	rs797045207(A;A)
Reference	Rs797045207(G;G)
Significance	Pathogenic
Disease	Persistent hyperinsulinemic hypoglycemia of infancy
Variation	info
Gene	ABCC8
CLNDBN	Persistent hyperinsulinemic hypoglycemia of infancy
Reversed	1
HGVS	NC_000011.9:g.17448702C>T
CLNSRC
CLNACC	RCV000194857.1,