rs1061651
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs1061651(A;G) |
Make rs1061651(G;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 12 |
Position | 114670556 |
Gene | TBX3 |
is a | snp |
is | mentioned by |
dbSNP | rs1061651 |
dbSNP (classic) | rs1061651 |
ClinGen | rs1061651 |
ebi | rs1061651 |
HLI | rs1061651 |
Exac | rs1061651 |
Gnomad | rs1061651 |
Varsome | rs1061651 |
LitVar | rs1061651 |
Map | rs1061651 |
PheGenI | rs1061651 |
Biobank | rs1061651 |
1000 genomes | rs1061651 |
hgdp | rs1061651 |
ensembl | rs1061651 |
geneview | rs1061651 |
scholar | rs1061651 |
rs1061651 | |
pharmgkb | rs1061651 |
gwascentral | rs1061651 |
openSNP | rs1061651 |
23andMe | rs1061651 |
SNPshot | rs1061651 |
SNPdbe | rs1061651 |
MSV3d | rs1061651 |
GWAS Ctlg | rs1061651 |
Max Magnitude | 0 |
[PMID 26920143] Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population.
ClinVar | |
---|---|
Risk | rs1061651(G;G) |
Alt | rs1061651(G;G) |
Reference | Rs1061651(A;A) |
Significance | Non-pathogenic |
Disease | Ulnar-mammary syndrome |
Variation | info |
Gene | TBX3 |
CLNDBN | Ulnar-mammary syndrome |
Reversed | 1 |
HGVS | NC_000012.11:g.115108361T>C |
CLNSRC | |
CLNACC | RCV000319833.1, |