rs863223517

Orientation

plus

Stabilized

plus

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

Make rs863223517(A;A)

Make rs863223517(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

74063374

Gene	ELN, LOC107986809

is a	snp
is	mentioned by
dbSNP	rs863223517
dbSNP (classic)	rs863223517
ClinGen	rs863223517
ebi	rs863223517
HLI	rs863223517
Exac	rs863223517
Gnomad	rs863223517
Varsome	rs863223517
LitVar	rs863223517
Map	rs863223517
PheGenI	rs863223517
Biobank	rs863223517
1000 genomes	rs863223517
hgdp	rs863223517
ensembl	rs863223517
geneview	rs863223517
scholar	rs863223517
google	rs863223517
pharmgkb	rs863223517
gwascentral	rs863223517
openSNP	rs863223517
23andMe	rs863223517
SNPshot	rs863223517
SNPdbe	rs863223517
MSV3d	rs863223517
GWAS Ctlg	rs863223517

Max Magnitude

0

ClinVar
Risk	rs863223517(A;A)
Alt	rs863223517(A;A)
Reference	Rs863223517(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ELN
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.73477704G>A
CLNSRC
CLNACC	RCV000200555.1,