rs1135401877
From SNPedia
Orientation | minus |
Make rs1135401877(-;-) |
Make rs1135401877(-;TCATT) |
Make rs1135401877(TCATT;TCATT) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 17 |
Position | 43074495 |
Gene | BRCA1 |
is a | snp |
is | mentioned by |
dbSNP | rs1135401877 |
dbSNP (classic) | rs1135401877 |
ClinGen | rs1135401877 |
ebi | rs1135401877 |
HLI | rs1135401877 |
Exac | rs1135401877 |
Gnomad | rs1135401877 |
Varsome | rs1135401877 |
LitVar | rs1135401877 |
Map | rs1135401877 |
PheGenI | rs1135401877 |
Biobank | rs1135401877 |
1000 genomes | rs1135401877 |
hgdp | rs1135401877 |
ensembl | rs1135401877 |
geneview | rs1135401877 |
scholar | rs1135401877 |
rs1135401877 | |
pharmgkb | rs1135401877 |
gwascentral | rs1135401877 |
openSNP | rs1135401877 |
23andMe | rs1135401877 |
SNPshot | rs1135401877 |
SNPdbe | rs1135401877 |
MSV3d | rs1135401877 |
GWAS Ctlg | rs1135401877 |
Max Magnitude | 0 |
aka NM_007294.3(BRCA1):c.4507_4511delTCATT or (p.Ser1503Argfs)
Pathogenic variant based on expert panel submission to ClinVar