rs387906407

Orientation

minus

Stabilized

minus

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

Make rs387906407(A;A)

Make rs387906407(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

17395610

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs387906407
dbSNP (classic)	rs387906407
ClinGen	rs387906407
ebi	rs387906407
HLI	rs387906407
Exac	rs387906407
Gnomad	rs387906407
Varsome	rs387906407
LitVar	rs387906407
Map	rs387906407
PheGenI	rs387906407
Biobank	rs387906407
1000 genomes	rs387906407
hgdp	rs387906407
ensembl	rs387906407
geneview	rs387906407
scholar	rs387906407
google	rs387906407
pharmgkb	rs387906407
gwascentral	rs387906407
openSNP	rs387906407
23andMe	rs387906407
SNPshot	rs387906407
SNPdbe	rs387906407
MSV3d	rs387906407
GWAS Ctlg	rs387906407

Max Magnitude

0

ClinVar
Risk	rs387906407(A;A)
Alt	rs387906407(A;A)
Reference	Rs387906407(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.17417157C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000009654.4,