rs144586521
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs144586521(C;T) |
Make rs144586521(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | X |
Position | 8536777 |
Gene | ANOS1 |
is a | snp |
is | mentioned by |
dbSNP | rs144586521 |
dbSNP (classic) | rs144586521 |
ClinGen | rs144586521 |
ebi | rs144586521 |
HLI | rs144586521 |
Exac | rs144586521 |
Gnomad | rs144586521 |
Varsome | rs144586521 |
LitVar | rs144586521 |
Map | rs144586521 |
PheGenI | rs144586521 |
Biobank | rs144586521 |
1000 genomes | rs144586521 |
hgdp | rs144586521 |
ensembl | rs144586521 |
geneview | rs144586521 |
scholar | rs144586521 |
rs144586521 | |
pharmgkb | rs144586521 |
gwascentral | rs144586521 |
openSNP | rs144586521 |
23andMe | rs144586521 |
SNPshot | rs144586521 |
SNPdbe | rs144586521 |
MSV3d | rs144586521 |
GWAS Ctlg | rs144586521 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs144586521(T;T) |
Alt | rs144586521(T;T) |
Reference | Rs144586521(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ANOS1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.8504818C>A |
CLNSRC | |
CLNACC | RCV000493134.1, |