rs863223515

Orientation

plus

Stabilized

plus

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

Make rs863223515(G;T)

Make rs863223515(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

74063176

Gene	ELN, LOC107986809

is a	snp
is	mentioned by
dbSNP	rs863223515
dbSNP (classic)	rs863223515
ClinGen	rs863223515
ebi	rs863223515
HLI	rs863223515
Exac	rs863223515
Gnomad	rs863223515
Varsome	rs863223515
LitVar	rs863223515
Map	rs863223515
PheGenI	rs863223515
Biobank	rs863223515
1000 genomes	rs863223515
hgdp	rs863223515
ensembl	rs863223515
geneview	rs863223515
scholar	rs863223515
google	rs863223515
pharmgkb	rs863223515
gwascentral	rs863223515
openSNP	rs863223515
23andMe	rs863223515
SNPshot	rs863223515
SNPdbe	rs863223515
MSV3d	rs863223515
GWAS Ctlg	rs863223515

Max Magnitude

0

ClinVar
Risk	rs863223515(T;T)
Alt	rs863223515(T;T)
Reference	Rs863223515(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ELN
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.73477506G>T
CLNSRC
CLNACC	RCV000196900.1,