rs387906408

Orientation

minus

Stabilized

minus

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

Make rs387906408(-;-)

Make rs387906408(-;TCC)

Make rs387906408(TCC;TCC)

Reference

GRCh38 38.1/141

Chromosome

11

Position

17395892

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs387906408
dbSNP (classic)	rs387906408
ClinGen	rs387906408
ebi	rs387906408
HLI	rs387906408
Exac	rs387906408
Gnomad	rs387906408
Varsome	rs387906408
LitVar	rs387906408
Map	rs387906408
PheGenI	rs387906408
Biobank	rs387906408
1000 genomes	rs387906408
hgdp	rs387906408
ensembl	rs387906408
geneview	rs387906408
scholar	rs387906408
google	rs387906408
pharmgkb	rs387906408
gwascentral	rs387906408
openSNP	rs387906408
23andMe	rs387906408
SNPshot	rs387906408
SNPdbe	rs387906408
MSV3d	rs387906408
GWAS Ctlg	rs387906408

Max Magnitude

0

ClinVar
Risk	rs387906408(-;-)
Alt	rs387906408(-;-)
Reference	Rs387906408(CCT;CCT)
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.17417439_17417441delGGA
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009668.3,