rs1064795608
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Chromosome | X |
Position | 41143432 |
Gene | USP9X |
is a | snp |
is | mentioned by |
dbSNP | rs1064795608 |
dbSNP (classic) | rs1064795608 |
ClinGen | rs1064795608 |
ebi | rs1064795608 |
HLI | rs1064795608 |
Exac | rs1064795608 |
Gnomad | rs1064795608 |
Varsome | rs1064795608 |
LitVar | rs1064795608 |
Map | rs1064795608 |
PheGenI | rs1064795608 |
Biobank | rs1064795608 |
1000 genomes | rs1064795608 |
hgdp | rs1064795608 |
ensembl | rs1064795608 |
geneview | rs1064795608 |
scholar | rs1064795608 |
rs1064795608 | |
pharmgkb | rs1064795608 |
gwascentral | rs1064795608 |
openSNP | rs1064795608 |
23andMe | rs1064795608 |
SNPshot | rs1064795608 |
SNPdbe | rs1064795608 |
MSV3d | rs1064795608 |
GWAS Ctlg | rs1064795608 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064795608(C;C) |
Alt | rs1064795608(C;C) |
Reference | Rs1064795608(T;T) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | USP9X |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.41002685T>C |
CLNSRC | |
CLNACC | RCV000482190.1, |