rs878853658

Orientation

minus

Stabilized

minus

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

Make rs878853658(-;-)

Make rs878853658(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

9

Position

127854289

Gene

ENG

is a	snp
is	mentioned by
dbSNP	rs878853658
dbSNP (classic)	rs878853658
ClinGen	rs878853658
ebi	rs878853658
HLI	rs878853658
Exac	rs878853658
Gnomad	rs878853658
Varsome	rs878853658
LitVar	rs878853658
Map	rs878853658
PheGenI	rs878853658
Biobank	rs878853658
1000 genomes	rs878853658
hgdp	rs878853658
ensembl	rs878853658
geneview	rs878853658
scholar	rs878853658
google	rs878853658
pharmgkb	rs878853658
gwascentral	rs878853658
openSNP	rs878853658
23andMe	rs878853658
SNPshot	rs878853658
SNPdbe	rs878853658
MSV3d	rs878853658
GWAS Ctlg	rs878853658

Max Magnitude

0

ClinVar
Risk	rs878853658(-;-)
Alt	rs878853658(-;-)
Reference	Rs878853658(A;A)
Significance	Pathogenic
Disease	Osler hemorrhagic telangiectasia syndrome
Variation	info
Gene	ENG
CLNDBN	Osler hemorrhagic telangiectasia syndrome
Reversed	1
HGVS	NC_000009.11:g.130616568delT
CLNSRC
CLNACC	RCV000228918.2,