rs587781527
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(GGAGGTC;GGAGGTC) | 0 | common in clinvar |
(GGAGGTC;TGAGGTT) | 6 | Ovarian cancer susceptibility |
Make rs587781527(TGAGGTT;TGAGGTT) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 17 |
Position | 35103466 |
Gene | RAD51D, RAD51L3-RFFL |
is a | snp |
is | mentioned by |
dbSNP | rs587781527 |
dbSNP (classic) | rs587781527 |
ClinGen | rs587781527 |
ebi | rs587781527 |
HLI | rs587781527 |
Exac | rs587781527 |
Gnomad | rs587781527 |
Varsome | rs587781527 |
LitVar | rs587781527 |
Map | rs587781527 |
PheGenI | rs587781527 |
Biobank | rs587781527 |
1000 genomes | rs587781527 |
hgdp | rs587781527 |
ensembl | rs587781527 |
geneview | rs587781527 |
scholar | rs587781527 |
rs587781527 | |
pharmgkb | rs587781527 |
gwascentral | rs587781527 |
openSNP | rs587781527 |
23andMe | rs587781527 |
SNPshot | rs587781527 |
SNPdbe | rs587781527 |
MSV3d | rs587781527 |
GWAS Ctlg | rs587781527 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs587781527(TGAGGTT;TGAGGTT) |
Alt | rs587781527(TGAGGTT;TGAGGTT) |
Reference | Rs587781527(GGAGGTC;GGAGGTC) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD51D RAD51L3-RFFL |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000017.10:g.33430485_33430491delGACCTCCinsAACCTCA |
CLNSRC | |
CLNACC | RCV000129520.1, |