rs863223528

Orientation

plus

Stabilized

plus

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

Make rs863223528(-;C)

Make rs863223528(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

74051798

Gene

ELN

is a	snp
is	mentioned by
dbSNP	rs863223528
dbSNP (classic)	rs863223528
ClinGen	rs863223528
ebi	rs863223528
HLI	rs863223528
Exac	rs863223528
Gnomad	rs863223528
Varsome	rs863223528
LitVar	rs863223528
Map	rs863223528
PheGenI	rs863223528
Biobank	rs863223528
1000 genomes	rs863223528
hgdp	rs863223528
ensembl	rs863223528
geneview	rs863223528
scholar	rs863223528
google	rs863223528
pharmgkb	rs863223528
gwascentral	rs863223528
openSNP	rs863223528
23andMe	rs863223528
SNPshot	rs863223528
SNPdbe	rs863223528
MSV3d	rs863223528
GWAS Ctlg	rs863223528

Max Magnitude

0

ClinVar
Risk	rs863223528(C;C)
Alt	rs863223528(C;C)
Reference	Rs863223528(-;-)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ELN
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.73466128dupC
CLNSRC
CLNACC	RCV000200220.1,