rs35441529
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs35441529(-;C) |
Make rs35441529(C;C) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 6 |
Position | 157206688 |
Gene | ARID1B |
is a | snp |
is | mentioned by |
dbSNP | rs35441529 |
dbSNP (classic) | rs35441529 |
ClinGen | rs35441529 |
ebi | rs35441529 |
HLI | rs35441529 |
Exac | rs35441529 |
Gnomad | rs35441529 |
Varsome | rs35441529 |
LitVar | rs35441529 |
Map | rs35441529 |
PheGenI | rs35441529 |
Biobank | rs35441529 |
1000 genomes | rs35441529 |
hgdp | rs35441529 |
ensembl | rs35441529 |
geneview | rs35441529 |
scholar | rs35441529 |
rs35441529 | |
pharmgkb | rs35441529 |
gwascentral | rs35441529 |
openSNP | rs35441529 |
23andMe | rs35441529 |
SNPshot | rs35441529 |
SNPdbe | rs35441529 |
MSV3d | rs35441529 |
GWAS Ctlg | rs35441529 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs35441529(C;C) |
Alt | rs35441529(C;C) |
Reference | Rs35441529(-;-) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ARID1B |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000006.11:g.157527822dupC |
CLNSRC | |
CLNACC | RCV000359978.1, |