rs527441189

Orientation

plus

Stabilized

plus

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

Make rs527441189(A;A)

Make rs527441189(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

74051764

Gene

ELN

is a	snp
is	mentioned by
dbSNP	rs527441189
dbSNP (classic)	rs527441189
ClinGen	rs527441189
ebi	rs527441189
HLI	rs527441189
Exac	rs527441189
Gnomad	rs527441189
Varsome	rs527441189
LitVar	rs527441189
Map	rs527441189
PheGenI	rs527441189
Biobank	rs527441189
1000 genomes	rs527441189
hgdp	rs527441189
ensembl	rs527441189
geneview	rs527441189
scholar	rs527441189
google	rs527441189
pharmgkb	rs527441189
gwascentral	rs527441189
openSNP	rs527441189
23andMe	rs527441189
SNPshot	rs527441189
SNPdbe	rs527441189
MSV3d	rs527441189
GWAS Ctlg	rs527441189

Max Magnitude

0

ClinVar
Risk	rs527441189(A;A)
Alt	rs527441189(A;A)
Reference	Rs527441189(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	ELN
CLNDBN	not provided
Reversed	0
HGVS	NC_000007.13:g.73466094G>T
CLNSRC
CLNACC	RCV000196542.1,