rs1085307432

Orientation

minus

Stabilized

minus

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

Chromosome

9

Position

127818810

Gene	ENG, LOC102723566

is a	snp
is	mentioned by
dbSNP	rs1085307432
dbSNP (classic)	rs1085307432
ClinGen	rs1085307432
ebi	rs1085307432
HLI	rs1085307432
Exac	rs1085307432
Gnomad	rs1085307432
Varsome	rs1085307432
LitVar	rs1085307432
Map	rs1085307432
PheGenI	rs1085307432
Biobank	rs1085307432
1000 genomes	rs1085307432
hgdp	rs1085307432
ensembl	rs1085307432
geneview	rs1085307432
scholar	rs1085307432
google	rs1085307432
pharmgkb	rs1085307432
gwascentral	rs1085307432
openSNP	rs1085307432
23andMe	rs1085307432
SNPshot	rs1085307432
SNPdbe	rs1085307432
MSV3d	rs1085307432
GWAS Ctlg	rs1085307432

Max Magnitude

0

ClinVar
Risk	rs1085307432(-;-)
Alt	rs1085307432(-;-)
Reference	Rs1085307432(T;T)
Significance	Pathogenic
Disease	Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia
Variation	info
Gene	ENG LOC102723566
CLNDBN	Pulmonary arterial hypertension related to hereditary hemorrhagic telangiectasia
Reversed	1
HGVS	NC_000009.11:g.130581089delA
CLNSRC
CLNACC	RCV000488464.1,