rs797045212

Orientation

minus

Stabilized

minus

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

Make rs797045212(-;GAGGCCACGGCTTCCATTGAC)

Make rs797045212(GAGGCCACGGCTTCCATTGAC;GAGGCCACGGCTTCCATTGAC)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

17394274

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs797045212
dbSNP (classic)	rs797045212
ClinGen	rs797045212
ebi	rs797045212
HLI	rs797045212
Exac	rs797045212
Gnomad	rs797045212
Varsome	rs797045212
LitVar	rs797045212
Map	rs797045212
PheGenI	rs797045212
Biobank	rs797045212
1000 genomes	rs797045212
hgdp	rs797045212
ensembl	rs797045212
geneview	rs797045212
scholar	rs797045212
google	rs797045212
pharmgkb	rs797045212
gwascentral	rs797045212
openSNP	rs797045212
23andMe	rs797045212
SNPshot	rs797045212
SNPdbe	rs797045212
MSV3d	rs797045212
GWAS Ctlg	rs797045212

Max Magnitude

0

ClinVar
Risk	rs797045212(GAGGCCACGGCTTCCATTGAC;GAGGCCACGGCTTCCATTGAC)
Alt	rs797045212(GAGGCCACGGCTTCCATTGAC;GAGGCCACGGCTTCCATTGAC)
Reference	Rs797045212(-;-)
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.17415822_17415842dup21
CLNSRC
CLNACC	RCV000193129.1,