rs863223511

Orientation

plus

Stabilized

plus

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

Make rs863223511(A;C)

Make rs863223511(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

74043116

Gene

ELN

is a	snp
is	mentioned by
dbSNP	rs863223511
dbSNP (classic)	rs863223511
ClinGen	rs863223511
ebi	rs863223511
HLI	rs863223511
Exac	rs863223511
Gnomad	rs863223511
Varsome	rs863223511
LitVar	rs863223511
Map	rs863223511
PheGenI	rs863223511
Biobank	rs863223511
1000 genomes	rs863223511
hgdp	rs863223511
ensembl	rs863223511
geneview	rs863223511
scholar	rs863223511
google	rs863223511
pharmgkb	rs863223511
gwascentral	rs863223511
openSNP	rs863223511
23andMe	rs863223511
SNPshot	rs863223511
SNPdbe	rs863223511
MSV3d	rs863223511
GWAS Ctlg	rs863223511

Max Magnitude

0

ClinVar
Risk	rs863223511(C;C)
Alt	rs863223511(C;C)
Reference	Rs863223511(A;A)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ELN
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.73457446A>C
CLNSRC
CLNACC	RCV000197464.1,