rs1060501949
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AAAGA;AAAGA) | 0 | common in clinvar |
Make rs1060501949(-;-) |
Make rs1060501949(-;AAAGA) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 132609345 |
Gene | RAD50 |
is a | snp |
is | mentioned by |
dbSNP | rs1060501949 |
dbSNP (classic) | rs1060501949 |
ClinGen | rs1060501949 |
ebi | rs1060501949 |
HLI | rs1060501949 |
Exac | rs1060501949 |
Gnomad | rs1060501949 |
Varsome | rs1060501949 |
LitVar | rs1060501949 |
Map | rs1060501949 |
PheGenI | rs1060501949 |
Biobank | rs1060501949 |
1000 genomes | rs1060501949 |
hgdp | rs1060501949 |
ensembl | rs1060501949 |
geneview | rs1060501949 |
scholar | rs1060501949 |
rs1060501949 | |
pharmgkb | rs1060501949 |
gwascentral | rs1060501949 |
openSNP | rs1060501949 |
23andMe | rs1060501949 |
SNPshot | rs1060501949 |
SNPdbe | rs1060501949 |
MSV3d | rs1060501949 |
GWAS Ctlg | rs1060501949 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1060501949(-;-) |
Alt | rs1060501949(-;-) |
Reference | Rs1060501949(AAAGA;AAAGA) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD50 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131945037_131945041delAAAGA |
CLNSRC | |
CLNACC | RCV000463503.1, |