rs587782866
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TTCCTGTGTCAGATA;TTCCTGTGTCAGATA) | 0 | common in clinvar |
Make rs587782866(-;-) |
Make rs587782866(-;CCTGTGTCAGATATT) |
Make rs587782866(CCTGTGTCAGATATT;CCTGTGTCAGATATT) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 132638071 |
Gene | RAD50, TH2LCRR |
is a | snp |
is | mentioned by |
dbSNP | rs587782866 |
dbSNP (classic) | rs587782866 |
ClinGen | rs587782866 |
ebi | rs587782866 |
HLI | rs587782866 |
Exac | rs587782866 |
Gnomad | rs587782866 |
Varsome | rs587782866 |
LitVar | rs587782866 |
Map | rs587782866 |
PheGenI | rs587782866 |
Biobank | rs587782866 |
1000 genomes | rs587782866 |
hgdp | rs587782866 |
ensembl | rs587782866 |
geneview | rs587782866 |
scholar | rs587782866 |
rs587782866 | |
pharmgkb | rs587782866 |
gwascentral | rs587782866 |
openSNP | rs587782866 |
23andMe | rs587782866 |
SNPshot | rs587782866 |
SNPdbe | rs587782866 |
MSV3d | rs587782866 |
GWAS Ctlg | rs587782866 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587782866(-;-) |
Alt | rs587782866(-;-) |
Reference | Rs587782866(TTCCTGTGTCAGATA;TTCCTGTGTCAGATA) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | LOC101927761 TH2LCRR RAD50 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131973763_131973777delCCTGTGTCAGATATT |
CLNSRC | |
CLNACC | RCV000132490.1, |