rs863223535

Orientation

minus

Stabilized

minus

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

Make rs863223535(C;C)

Make rs863223535(C;T)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

127825693

Gene	ENG, LOC105379841

is a	snp
is	mentioned by
dbSNP	rs863223535
dbSNP (classic)	rs863223535
ClinGen	rs863223535
ebi	rs863223535
HLI	rs863223535
Exac	rs863223535
Gnomad	rs863223535
Varsome	rs863223535
LitVar	rs863223535
Map	rs863223535
PheGenI	rs863223535
Biobank	rs863223535
1000 genomes	rs863223535
hgdp	rs863223535
ensembl	rs863223535
geneview	rs863223535
scholar	rs863223535
google	rs863223535
pharmgkb	rs863223535
gwascentral	rs863223535
openSNP	rs863223535
23andMe	rs863223535
SNPshot	rs863223535
SNPdbe	rs863223535
MSV3d	rs863223535
GWAS Ctlg	rs863223535

Max Magnitude

0

ClinVar
Risk	rs863223535(C;C)
Alt	rs863223535(C;C)
Reference	Rs863223535(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ENG
CLNDBN	not provided
Reversed	1
HGVS	NC_000009.11:g.130587972A>G
CLNSRC
CLNACC	RCV000200037.1,