rs750586158
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs750586158(C;T) |
Make rs750586158(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 132638203 |
Gene | RAD50, TH2LCRR |
is a | snp |
is | mentioned by |
dbSNP | rs750586158 |
dbSNP (classic) | rs750586158 |
ClinGen | rs750586158 |
ebi | rs750586158 |
HLI | rs750586158 |
Exac | rs750586158 |
Gnomad | rs750586158 |
Varsome | rs750586158 |
LitVar | rs750586158 |
Map | rs750586158 |
PheGenI | rs750586158 |
Biobank | rs750586158 |
1000 genomes | rs750586158 |
hgdp | rs750586158 |
ensembl | rs750586158 |
geneview | rs750586158 |
scholar | rs750586158 |
rs750586158 | |
pharmgkb | rs750586158 |
gwascentral | rs750586158 |
openSNP | rs750586158 |
23andMe | rs750586158 |
SNPshot | rs750586158 |
SNPdbe | rs750586158 |
MSV3d | rs750586158 |
GWAS Ctlg | rs750586158 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs750586158(T;T) |
Alt | rs750586158(T;T) |
Reference | Rs750586158(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | LOC101927761 TH2LCRR RAD50 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131973895C>T |
CLNSRC | |
CLNACC | RCV000164215.3, |