rs782238674

Orientation

plus

Stabilized

plus

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

Make rs782238674(A;A)

Make rs782238674(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

74051840

Gene

ELN

is a	snp
is	mentioned by
dbSNP	rs782238674
dbSNP (classic)	rs782238674
ClinGen	rs782238674
ebi	rs782238674
HLI	rs782238674
Exac	rs782238674
Gnomad	rs782238674
Varsome	rs782238674
LitVar	rs782238674
Map	rs782238674
PheGenI	rs782238674
Biobank	rs782238674
1000 genomes	rs782238674
hgdp	rs782238674
ensembl	rs782238674
geneview	rs782238674
scholar	rs782238674
google	rs782238674
pharmgkb	rs782238674
gwascentral	rs782238674
openSNP	rs782238674
23andMe	rs782238674
SNPshot	rs782238674
SNPdbe	rs782238674
MSV3d	rs782238674
GWAS Ctlg	rs782238674

Max Magnitude

0

ClinVar
Risk	rs782238674(A;A) rs782238674(T;T)
Alt	rs782238674(A;A) rs782238674(T;T)
Reference	Rs782238674(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ELN
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.73466170G>A
CLNSRC
CLNACC	RCV000479896.1,