rs863223534

Orientation

minus

Stabilized

minus

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

Make rs863223534(A;A)

Make rs863223534(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

127826587

Gene	ENG, LOC105379841

is a	snp
is	mentioned by
dbSNP	rs863223534
dbSNP (classic)	rs863223534
ClinGen	rs863223534
ebi	rs863223534
HLI	rs863223534
Exac	rs863223534
Gnomad	rs863223534
Varsome	rs863223534
LitVar	rs863223534
Map	rs863223534
PheGenI	rs863223534
Biobank	rs863223534
1000 genomes	rs863223534
hgdp	rs863223534
ensembl	rs863223534
geneview	rs863223534
scholar	rs863223534
google	rs863223534
pharmgkb	rs863223534
gwascentral	rs863223534
openSNP	rs863223534
23andMe	rs863223534
SNPshot	rs863223534
SNPdbe	rs863223534
MSV3d	rs863223534
GWAS Ctlg	rs863223534

Max Magnitude

0

ClinVar
Risk	rs863223534(A;A)
Alt	rs863223534(A;A)
Reference	Rs863223534(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ENG
CLNDBN	not provided
Reversed	1
HGVS	NC_000009.11:g.130588866C>T
CLNSRC
CLNACC	RCV000195747.1,