rs863223514

Orientation

plus

Stabilized

plus

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

Make rs863223514(G;T)

Make rs863223514(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

74061106

Gene	ELN, LOC107986809

is a	snp
is	mentioned by
dbSNP	rs863223514
dbSNP (classic)	rs863223514
ClinGen	rs863223514
ebi	rs863223514
HLI	rs863223514
Exac	rs863223514
Gnomad	rs863223514
Varsome	rs863223514
LitVar	rs863223514
Map	rs863223514
PheGenI	rs863223514
Biobank	rs863223514
1000 genomes	rs863223514
hgdp	rs863223514
ensembl	rs863223514
geneview	rs863223514
scholar	rs863223514
google	rs863223514
pharmgkb	rs863223514
gwascentral	rs863223514
openSNP	rs863223514
23andMe	rs863223514
SNPshot	rs863223514
SNPdbe	rs863223514
MSV3d	rs863223514
GWAS Ctlg	rs863223514

Max Magnitude

0

ClinVar
Risk	rs863223514(T;T)
Alt	rs863223514(T;T)
Reference	Rs863223514(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ELN
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.73475436G>T
CLNSRC
CLNACC	RCV000200864.1,