rs886041471
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(GGCTTCGTGGTCTTCTCCATCCTG;GGCTTCGTGGTCTTCTCCATCCTG) | 0 | common in clinvar |
Chromosome | X |
Position | 153693517 |
Gene | SLC6A8 |
is a | snp |
is | mentioned by |
dbSNP | rs886041471 |
dbSNP (classic) | rs886041471 |
ClinGen | rs886041471 |
ebi | rs886041471 |
HLI | rs886041471 |
Exac | rs886041471 |
Gnomad | rs886041471 |
Varsome | rs886041471 |
LitVar | rs886041471 |
Map | rs886041471 |
PheGenI | rs886041471 |
Biobank | rs886041471 |
1000 genomes | rs886041471 |
hgdp | rs886041471 |
ensembl | rs886041471 |
geneview | rs886041471 |
scholar | rs886041471 |
rs886041471 | |
pharmgkb | rs886041471 |
gwascentral | rs886041471 |
openSNP | rs886041471 |
23andMe | rs886041471 |
SNPshot | rs886041471 |
SNPdbe | rs886041471 |
MSV3d | rs886041471 |
GWAS Ctlg | rs886041471 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886041471(-;-) |
Alt | rs886041471(-;-) |
Reference | Rs886041471(GGCTTCGTGGTCTTCTCCATCCTG;GGCTTCGTGGTCTTCTCCATCCTG) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC6A8 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.152958972_152958995del24 |
CLNSRC | |
CLNACC | RCV000370906.1, |