rs11545664

Orientation

minus

Stabilized

minus

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

Make rs11545664(A;A)

Make rs11545664(A;G)

Reference

GRCh38 38.1/142

Chromosome

9

Position

127843106

Gene

ENG

is a	snp
is	mentioned by
dbSNP	rs11545664
dbSNP (classic)	rs11545664
ClinGen	rs11545664
ebi	rs11545664
HLI	rs11545664
Exac	rs11545664
Gnomad	rs11545664
Varsome	rs11545664
LitVar	rs11545664
Map	rs11545664
PheGenI	rs11545664
Biobank	rs11545664
1000 genomes	rs11545664
hgdp	rs11545664
ensembl	rs11545664
geneview	rs11545664
scholar	rs11545664
google	rs11545664
pharmgkb	rs11545664
gwascentral	rs11545664
openSNP	rs11545664
23andMe	rs11545664
SNPshot	rs11545664
SNPdbe	rs11545664
MSV3d	rs11545664
GWAS Ctlg	rs11545664

Merged from

Rs16930129

GMAF

0.1249

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

ClinVar
Risk	rs11545664(A;A)
Alt	rs11545664(A;A)
Reference	Rs11545664(G;G)
Significance	Probable-non-pathogenic
Disease	not specified Juvenile Polyposis Osler hemorrhagic telangiectasia syndrome
Variation	info
Gene	ENG
CLNDBN	not specified Juvenile Polyposis Osler hemorrhagic telangiectasia syndrome
Reversed	1
HGVS	NC_000009.11:g.130605385C>T
CLNSRC	ClinVar GeneDx
CLNACC	RCV000150652.4, RCV000273604.1, RCV000368171.1,