rs878854423
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs878854423(-;C) |
Make rs878854423(C;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | X |
Position | 74743931 |
Gene | KIAA2022 |
is a | snp |
is | mentioned by |
dbSNP | rs878854423 |
dbSNP (classic) | rs878854423 |
ClinGen | rs878854423 |
ebi | rs878854423 |
HLI | rs878854423 |
Exac | rs878854423 |
Gnomad | rs878854423 |
Varsome | rs878854423 |
LitVar | rs878854423 |
Map | rs878854423 |
PheGenI | rs878854423 |
Biobank | rs878854423 |
1000 genomes | rs878854423 |
hgdp | rs878854423 |
ensembl | rs878854423 |
geneview | rs878854423 |
scholar | rs878854423 |
rs878854423 | |
pharmgkb | rs878854423 |
gwascentral | rs878854423 |
openSNP | rs878854423 |
23andMe | rs878854423 |
SNPshot | rs878854423 |
SNPdbe | rs878854423 |
MSV3d | rs878854423 |
GWAS Ctlg | rs878854423 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878854423(C;C) |
Alt | rs878854423(C;C) |
Reference | Rs878854423(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | KIAA2022 |
CLNDBN | not provided |
Reversed | 1 |
HGVS | NC_000023.10:g.73963767dupG |
CLNSRC | |
CLNACC | RCV000231539.1, |