rs867328327
From SNPedia
Merged into | rs587781625 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs867328327(-;A) |
Make rs867328327(A;A) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 5 |
Position | 132557417 |
Gene | IL5, RAD50 |
is a | snp |
is | mentioned by |
dbSNP | rs867328327 |
dbSNP (classic) | rs867328327 |
ClinGen | rs867328327 |
ebi | rs867328327 |
HLI | rs867328327 |
Exac | rs867328327 |
Gnomad | rs867328327 |
Varsome | rs867328327 |
LitVar | rs867328327 |
Map | rs867328327 |
PheGenI | rs867328327 |
Biobank | rs867328327 |
1000 genomes | rs867328327 |
hgdp | rs867328327 |
ensembl | rs867328327 |
geneview | rs867328327 |
scholar | rs867328327 |
rs867328327 | |
pharmgkb | rs867328327 |
gwascentral | rs867328327 |
openSNP | rs867328327 |
23andMe | rs867328327 |
SNPshot | rs867328327 |
SNPdbe | rs867328327 |
MSV3d | rs867328327 |
GWAS Ctlg | rs867328327 |
Status | Merged into rs587781625 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs867328327(A;A) |
Alt | rs867328327(A;A) |
Reference | Rs867328327(;) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD50 IL5 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131893110dupA |
CLNSRC | |
CLNACC | RCV000129727.3, |