rs879255333
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AGGAATTTGC;AGGAATTTGC) | 0 | common in clinvar |
Make rs879255333(-;-) |
Make rs879255333(-;AGGAATTTGC) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 13 |
Position | 32362636 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs879255333 |
dbSNP (classic) | rs879255333 |
ClinGen | rs879255333 |
ebi | rs879255333 |
HLI | rs879255333 |
Exac | rs879255333 |
Gnomad | rs879255333 |
Varsome | rs879255333 |
LitVar | rs879255333 |
Map | rs879255333 |
PheGenI | rs879255333 |
Biobank | rs879255333 |
1000 genomes | rs879255333 |
hgdp | rs879255333 |
ensembl | rs879255333 |
geneview | rs879255333 |
scholar | rs879255333 |
rs879255333 | |
pharmgkb | rs879255333 |
gwascentral | rs879255333 |
openSNP | rs879255333 |
23andMe | rs879255333 |
SNPshot | rs879255333 |
SNPdbe | rs879255333 |
MSV3d | rs879255333 |
GWAS Ctlg | rs879255333 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs879255333(-;-) |
Alt | rs879255333(-;-) |
Reference | Rs879255333(AGGAATTTGC;AGGAATTTGC) |
Significance | Probable-Pathogenic |
Disease | not specified |
Variation | info |
Gene | BRCA2 |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000013.10:g.32936773_32936782delAGGAATTTGC |
CLNSRC | |
CLNACC | RCV000239178.1, |