rs748086984
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs748086984(A;A) |
Make rs748086984(A;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 5 |
Position | 132557455 |
Gene | IL5, RAD50 |
is a | snp |
is | mentioned by |
dbSNP | rs748086984 |
dbSNP (classic) | rs748086984 |
ClinGen | rs748086984 |
ebi | rs748086984 |
HLI | rs748086984 |
Exac | rs748086984 |
Gnomad | rs748086984 |
Varsome | rs748086984 |
LitVar | rs748086984 |
Map | rs748086984 |
PheGenI | rs748086984 |
Biobank | rs748086984 |
1000 genomes | rs748086984 |
hgdp | rs748086984 |
ensembl | rs748086984 |
geneview | rs748086984 |
scholar | rs748086984 |
rs748086984 | |
pharmgkb | rs748086984 |
gwascentral | rs748086984 |
openSNP | rs748086984 |
23andMe | rs748086984 |
SNPshot | rs748086984 |
SNPdbe | rs748086984 |
MSV3d | rs748086984 |
GWAS Ctlg | rs748086984 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs748086984(A;A) |
Alt | rs748086984(A;A) |
Reference | Rs748086984(T;T) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD50 IL5 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131893147T>A |
CLNSRC | |
CLNACC | RCV000216511.1, |