rs1064793575
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TG;TG) | 0 | common in clinvar |
Chromosome | X |
Position | 136016707 |
Gene | SLC9A6 |
is a | snp |
is | mentioned by |
dbSNP | rs1064793575 |
dbSNP (classic) | rs1064793575 |
ClinGen | rs1064793575 |
ebi | rs1064793575 |
HLI | rs1064793575 |
Exac | rs1064793575 |
Gnomad | rs1064793575 |
Varsome | rs1064793575 |
LitVar | rs1064793575 |
Map | rs1064793575 |
PheGenI | rs1064793575 |
Biobank | rs1064793575 |
1000 genomes | rs1064793575 |
hgdp | rs1064793575 |
ensembl | rs1064793575 |
geneview | rs1064793575 |
scholar | rs1064793575 |
rs1064793575 | |
pharmgkb | rs1064793575 |
gwascentral | rs1064793575 |
openSNP | rs1064793575 |
23andMe | rs1064793575 |
SNPshot | rs1064793575 |
SNPdbe | rs1064793575 |
MSV3d | rs1064793575 |
GWAS Ctlg | rs1064793575 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1064793575(-;-) |
Alt | rs1064793575(-;-) |
Reference | Rs1064793575(TG;TG) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC9A6 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.135098866_135098867delGT |
CLNSRC | |
CLNACC | RCV000482382.1, |