rs753023295
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs753023295(C;T) |
Make rs753023295(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 17 |
Position | 61780858 |
Gene | BRIP1 |
is a | snp |
is | mentioned by |
dbSNP | rs753023295 |
dbSNP (classic) | rs753023295 |
ClinGen | rs753023295 |
ebi | rs753023295 |
HLI | rs753023295 |
Exac | rs753023295 |
Gnomad | rs753023295 |
Varsome | rs753023295 |
LitVar | rs753023295 |
Map | rs753023295 |
PheGenI | rs753023295 |
Biobank | rs753023295 |
1000 genomes | rs753023295 |
hgdp | rs753023295 |
ensembl | rs753023295 |
geneview | rs753023295 |
scholar | rs753023295 |
rs753023295 | |
pharmgkb | rs753023295 |
gwascentral | rs753023295 |
openSNP | rs753023295 |
23andMe | rs753023295 |
SNPshot | rs753023295 |
SNPdbe | rs753023295 |
MSV3d | rs753023295 |
GWAS Ctlg | rs753023295 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs753023295(T;T) |
Alt | rs753023295(T;T) |
Reference | Rs753023295(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | BRIP1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000017.10:g.59858219C>T |
CLNSRC | |
CLNACC | RCV000215063.2, |