rs863223522

Orientation

plus

Stabilized

plus

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

Make rs863223522(-;-)

Make rs863223522(-;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

74056315

Gene

ELN

is a	snp
is	mentioned by
dbSNP	rs863223522
dbSNP (classic)	rs863223522
ClinGen	rs863223522
ebi	rs863223522
HLI	rs863223522
Exac	rs863223522
Gnomad	rs863223522
Varsome	rs863223522
LitVar	rs863223522
Map	rs863223522
PheGenI	rs863223522
Biobank	rs863223522
1000 genomes	rs863223522
hgdp	rs863223522
ensembl	rs863223522
geneview	rs863223522
scholar	rs863223522
google	rs863223522
pharmgkb	rs863223522
gwascentral	rs863223522
openSNP	rs863223522
23andMe	rs863223522
SNPshot	rs863223522
SNPdbe	rs863223522
MSV3d	rs863223522
GWAS Ctlg	rs863223522

Max Magnitude

0

ClinVar
Risk	rs863223522(-;-)
Alt	rs863223522(-;-)
Reference	Rs863223522(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ELN
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.73470645delG
CLNSRC
CLNACC	RCV000200111.1,