rs863223542

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(A;G)	4.3	Hereditary hemorrhagic telangiectasia
(G;G)	0	common in clinvar

Make rs863223542(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

127818715

Gene	ENG, LOC102723566

is a	snp
is	mentioned by
dbSNP	rs863223542
dbSNP (classic)	rs863223542
ClinGen	rs863223542
ebi	rs863223542
HLI	rs863223542
Exac	rs863223542
Gnomad	rs863223542
Varsome	rs863223542
LitVar	rs863223542
Map	rs863223542
PheGenI	rs863223542
Biobank	rs863223542
1000 genomes	rs863223542
hgdp	rs863223542
ensembl	rs863223542
geneview	rs863223542
scholar	rs863223542
google	rs863223542
pharmgkb	rs863223542
gwascentral	rs863223542
openSNP	rs863223542
23andMe	rs863223542
SNPshot	rs863223542
SNPdbe	rs863223542
MSV3d	rs863223542
GWAS Ctlg	rs863223542

Max Magnitude

4.3

ClinVar
Risk	rs863223542(A;A)
Alt	rs863223542(A;A)
Reference	Rs863223542(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ENG LOC102723566
CLNDBN	not provided
Reversed	1
HGVS	NC_000009.11:g.130580994C>T
CLNSRC
CLNACC	RCV000198224.1,