rs527441189
From SNPedia
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 |
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, |