rs782755390

Orientation

plus

Stabilized

plus

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

Make rs782755390(C;T)

Make rs782755390(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

74068650

Gene

ELN

is a	snp
is	mentioned by
dbSNP	rs782755390
dbSNP (classic)	rs782755390
ClinGen	rs782755390
ebi	rs782755390
HLI	rs782755390
Exac	rs782755390
Gnomad	rs782755390
Varsome	rs782755390
LitVar	rs782755390
Map	rs782755390
PheGenI	rs782755390
Biobank	rs782755390
1000 genomes	rs782755390
hgdp	rs782755390
ensembl	rs782755390
geneview	rs782755390
scholar	rs782755390
google	rs782755390
pharmgkb	rs782755390
gwascentral	rs782755390
openSNP	rs782755390
23andMe	rs782755390
SNPshot	rs782755390
SNPdbe	rs782755390
MSV3d	rs782755390
GWAS Ctlg	rs782755390

Max Magnitude

0

ClinVar
Risk	rs782755390(A;A) rs782755390(T;T)
Alt	rs782755390(A;A) rs782755390(T;T)
Reference	Rs782755390(C;C)
Significance	Probable-Pathogenic
Disease	not specified
Variation	info
Gene	ELN
CLNDBN	not specified
Reversed	0
HGVS	NC_000007.13:g.73482980C>A
CLNSRC
CLNACC	RCV000198856.2,