rs775069541
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs775069541(G;G) |
Make rs775069541(G;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 5 |
Position | 132618277 |
Gene | RAD50 |
is a | snp |
is | mentioned by |
dbSNP | rs775069541 |
dbSNP (classic) | rs775069541 |
ClinGen | rs775069541 |
ebi | rs775069541 |
HLI | rs775069541 |
Exac | rs775069541 |
Gnomad | rs775069541 |
Varsome | rs775069541 |
LitVar | rs775069541 |
Map | rs775069541 |
PheGenI | rs775069541 |
Biobank | rs775069541 |
1000 genomes | rs775069541 |
hgdp | rs775069541 |
ensembl | rs775069541 |
geneview | rs775069541 |
scholar | rs775069541 |
rs775069541 | |
pharmgkb | rs775069541 |
gwascentral | rs775069541 |
openSNP | rs775069541 |
23andMe | rs775069541 |
SNPshot | rs775069541 |
SNPdbe | rs775069541 |
MSV3d | rs775069541 |
GWAS Ctlg | rs775069541 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs775069541(A;A) rs775069541(G;G) |
Alt | rs775069541(A;A) rs775069541(G;G) |
Reference | Rs775069541(T;T) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD50 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131953969T>A |
CLNSRC | |
CLNACC | RCV000218193.1, |