rs863223516

Orientation

plus

Stabilized

plus

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

Make rs863223516(A;A)

Make rs863223516(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

74063309

Gene	ELN, LOC107986809

is a	snp
is	mentioned by
dbSNP	rs863223516
dbSNP (classic)	rs863223516
ClinGen	rs863223516
ebi	rs863223516
HLI	rs863223516
Exac	rs863223516
Gnomad	rs863223516
Varsome	rs863223516
LitVar	rs863223516
Map	rs863223516
PheGenI	rs863223516
Biobank	rs863223516
1000 genomes	rs863223516
hgdp	rs863223516
ensembl	rs863223516
geneview	rs863223516
scholar	rs863223516
google	rs863223516
pharmgkb	rs863223516
gwascentral	rs863223516
openSNP	rs863223516
23andMe	rs863223516
SNPshot	rs863223516
SNPdbe	rs863223516
MSV3d	rs863223516
GWAS Ctlg	rs863223516

Max Magnitude

0

ClinVar
Risk	rs863223516(A;A)
Alt	rs863223516(A;A)
Reference	Rs863223516(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ELN
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.73477639G>A
CLNSRC
CLNACC	RCV000199115.3,