rs782096458

Orientation

plus

Stabilized

plus

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

Make rs782096458(A;C)

Make rs782096458(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

74037705

Gene

ELN

is a	snp
is	mentioned by
dbSNP	rs782096458
dbSNP (classic)	rs782096458
ClinGen	rs782096458
ebi	rs782096458
HLI	rs782096458
Exac	rs782096458
Gnomad	rs782096458
Varsome	rs782096458
LitVar	rs782096458
Map	rs782096458
PheGenI	rs782096458
Biobank	rs782096458
1000 genomes	rs782096458
hgdp	rs782096458
ensembl	rs782096458
geneview	rs782096458
scholar	rs782096458
google	rs782096458
pharmgkb	rs782096458
gwascentral	rs782096458
openSNP	rs782096458
23andMe	rs782096458
SNPshot	rs782096458
SNPdbe	rs782096458
MSV3d	rs782096458
GWAS Ctlg	rs782096458

Max Magnitude

0

ClinVar
Risk	rs782096458(C;C)
Alt	rs782096458(C;C)
Reference	Rs782096458(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ELN
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.73452035A>C
CLNSRC
CLNACC	RCV000430802.1,