rs863223521

Orientation

plus

Stabilized

plus

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

Make rs863223521(-;-)

Make rs863223521(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

74056281

Gene

ELN

is a	snp
is	mentioned by
dbSNP	rs863223521
dbSNP (classic)	rs863223521
ClinGen	rs863223521
ebi	rs863223521
HLI	rs863223521
Exac	rs863223521
Gnomad	rs863223521
Varsome	rs863223521
LitVar	rs863223521
Map	rs863223521
PheGenI	rs863223521
Biobank	rs863223521
1000 genomes	rs863223521
hgdp	rs863223521
ensembl	rs863223521
geneview	rs863223521
scholar	rs863223521
google	rs863223521
pharmgkb	rs863223521
gwascentral	rs863223521
openSNP	rs863223521
23andMe	rs863223521
SNPshot	rs863223521
SNPdbe	rs863223521
MSV3d	rs863223521
GWAS Ctlg	rs863223521

Max Magnitude

0

ClinVar
Risk	rs863223521(-;-)
Alt	rs863223521(-;-)
Reference	Rs863223521(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ELN
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.73470611delC
CLNSRC
CLNACC	RCV000197682.1,