rs863223512

Orientation

plus

Stabilized

plus

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

Make rs863223512(A;A)

Make rs863223512(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

74043117

Gene

ELN

is a	snp
is	mentioned by
dbSNP	rs863223512
dbSNP (classic)	rs863223512
ClinGen	rs863223512
ebi	rs863223512
HLI	rs863223512
Exac	rs863223512
Gnomad	rs863223512
Varsome	rs863223512
LitVar	rs863223512
Map	rs863223512
PheGenI	rs863223512
Biobank	rs863223512
1000 genomes	rs863223512
hgdp	rs863223512
ensembl	rs863223512
geneview	rs863223512
scholar	rs863223512
google	rs863223512
pharmgkb	rs863223512
gwascentral	rs863223512
openSNP	rs863223512
23andMe	rs863223512
SNPshot	rs863223512
SNPdbe	rs863223512
MSV3d	rs863223512
GWAS Ctlg	rs863223512

Max Magnitude

0

ClinVar
Risk	rs863223512(A;A)
Alt	rs863223512(A;A)
Reference	Rs863223512(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ELN
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.73457447G>A
CLNSRC
CLNACC	RCV000199726.1,