rs796053297
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CA;CA) | 0 | common in clinvar |
Make rs796053297(-;-) |
Make rs796053297(-;CA) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 136010495 |
Gene | SLC9A6 |
is a | snp |
is | mentioned by |
dbSNP | rs796053297 |
dbSNP (classic) | rs796053297 |
ClinGen | rs796053297 |
ebi | rs796053297 |
HLI | rs796053297 |
Exac | rs796053297 |
Gnomad | rs796053297 |
Varsome | rs796053297 |
LitVar | rs796053297 |
Map | rs796053297 |
PheGenI | rs796053297 |
Biobank | rs796053297 |
1000 genomes | rs796053297 |
hgdp | rs796053297 |
ensembl | rs796053297 |
geneview | rs796053297 |
scholar | rs796053297 |
rs796053297 | |
pharmgkb | rs796053297 |
gwascentral | rs796053297 |
openSNP | rs796053297 |
23andMe | rs796053297 |
SNPshot | rs796053297 |
SNPdbe | rs796053297 |
MSV3d | rs796053297 |
GWAS Ctlg | rs796053297 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs796053297(-;-) |
Alt | rs796053297(-;-) |
Reference | Rs796053297(CA;CA) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | SLC9A6 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000023.10:g.135092654_135092655delCA |
CLNSRC | |
CLNACC | RCV000189424.2, |