rs863223513

Orientation

plus

Stabilized

plus

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

Make rs863223513(A;A)

Make rs863223513(A;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

74046742

Gene

ELN

is a	snp
is	mentioned by
dbSNP	rs863223513
dbSNP (classic)	rs863223513
ClinGen	rs863223513
ebi	rs863223513
HLI	rs863223513
Exac	rs863223513
Gnomad	rs863223513
Varsome	rs863223513
LitVar	rs863223513
Map	rs863223513
PheGenI	rs863223513
Biobank	rs863223513
1000 genomes	rs863223513
hgdp	rs863223513
ensembl	rs863223513
geneview	rs863223513
scholar	rs863223513
google	rs863223513
pharmgkb	rs863223513
gwascentral	rs863223513
openSNP	rs863223513
23andMe	rs863223513
SNPshot	rs863223513
SNPdbe	rs863223513
MSV3d	rs863223513
GWAS Ctlg	rs863223513

Max Magnitude

0

ClinVar
Risk	rs863223513(A;A)
Alt	rs863223513(A;A)
Reference	Rs863223513(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ELN
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.73461072T>A
CLNSRC
CLNACC	RCV000196516.2,