rs886039525
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CAA;CAA) | 0 | common in clinvar |
Make rs886039525(-;-) |
Make rs886039525(-;AAC) |
Make rs886039525(AAC;AAC) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | X |
Position | 153693356 |
Gene | SLC6A8 |
is a | snp |
is | mentioned by |
dbSNP | rs886039525 |
dbSNP (classic) | rs886039525 |
ClinGen | rs886039525 |
ebi | rs886039525 |
HLI | rs886039525 |
Exac | rs886039525 |
Gnomad | rs886039525 |
Varsome | rs886039525 |
LitVar | rs886039525 |
Map | rs886039525 |
PheGenI | rs886039525 |
Biobank | rs886039525 |
1000 genomes | rs886039525 |
hgdp | rs886039525 |
ensembl | rs886039525 |
geneview | rs886039525 |
scholar | rs886039525 |
rs886039525 | |
pharmgkb | rs886039525 |
gwascentral | rs886039525 |
openSNP | rs886039525 |
23andMe | rs886039525 |
SNPshot | rs886039525 |
SNPdbe | rs886039525 |
MSV3d | rs886039525 |
GWAS Ctlg | rs886039525 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886039525(-;-) |
Alt | rs886039525(-;-) |
Reference | Rs886039525(CAA;CAA) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC6A8 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.152958811_152958813delAAC |
CLNSRC | |
CLNACC | RCV000255812.1, |