rs139964066

Orientation

plus

Stabilized

plus

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

Make rs139964066(A;A)

Make rs139964066(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

17402671

Gene

ABCC8

is a	snp
is	mentioned by
dbSNP	rs139964066
dbSNP (classic)	rs139964066
ClinGen	rs139964066
ebi	rs139964066
HLI	rs139964066
Exac	rs139964066
Gnomad	rs139964066
Varsome	rs139964066
LitVar	rs139964066
Map	rs139964066
PheGenI	rs139964066
Biobank	rs139964066
1000 genomes	rs139964066
hgdp	rs139964066
ensembl	rs139964066
geneview	rs139964066
scholar	rs139964066
google	rs139964066
pharmgkb	rs139964066
gwascentral	rs139964066
openSNP	rs139964066
23andMe	rs139964066
SNPshot	rs139964066
SNPdbe	rs139964066
MSV3d	rs139964066
GWAS Ctlg	rs139964066

Max Magnitude

0

ClinVar
Risk	rs139964066(A;A)
Alt	rs139964066(A;A)
Reference	Rs139964066(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ABCC8
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.17424218G>A
CLNSRC
CLNACC	RCV000223959.1,