rs863223537

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;C)	0	common in clinvar
(C;T)	4.3	Hereditary hemorrhagic telangiectasia

Make rs863223537(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

127825822

Gene	ENG, LOC105379841

is a	snp
is	mentioned by
dbSNP	rs863223537
dbSNP (classic)	rs863223537
ClinGen	rs863223537
ebi	rs863223537
HLI	rs863223537
Exac	rs863223537
Gnomad	rs863223537
Varsome	rs863223537
LitVar	rs863223537
Map	rs863223537
PheGenI	rs863223537
Biobank	rs863223537
1000 genomes	rs863223537
hgdp	rs863223537
ensembl	rs863223537
geneview	rs863223537
scholar	rs863223537
google	rs863223537
pharmgkb	rs863223537
gwascentral	rs863223537
openSNP	rs863223537
23andMe	rs863223537
SNPshot	rs863223537
SNPdbe	rs863223537
MSV3d	rs863223537
GWAS Ctlg	rs863223537

Max Magnitude

4.3

ClinVar
Risk	rs863223537(T;T)
Alt	rs863223537(T;T)
Reference	Rs863223537(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ENG
CLNDBN	not provided
Reversed	1
HGVS	NC_000009.11:g.130588101G>A
CLNSRC
CLNACC	RCV000199857.2,