rs1135401874
From SNPedia
Orientation | minus |
Make rs1135401874(-;-) |
Make rs1135401874(-;C) |
Make rs1135401874(C;C) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 17 |
Position | 43082451 |
Gene | BRCA1 |
is a | snp |
is | mentioned by |
dbSNP | rs1135401874 |
dbSNP (classic) | rs1135401874 |
ClinGen | rs1135401874 |
ebi | rs1135401874 |
HLI | rs1135401874 |
Exac | rs1135401874 |
Gnomad | rs1135401874 |
Varsome | rs1135401874 |
LitVar | rs1135401874 |
Map | rs1135401874 |
PheGenI | rs1135401874 |
Biobank | rs1135401874 |
1000 genomes | rs1135401874 |
hgdp | rs1135401874 |
ensembl | rs1135401874 |
geneview | rs1135401874 |
scholar | rs1135401874 |
rs1135401874 | |
pharmgkb | rs1135401874 |
gwascentral | rs1135401874 |
openSNP | rs1135401874 |
23andMe | rs1135401874 |
SNPshot | rs1135401874 |
SNPdbe | rs1135401874 |
MSV3d | rs1135401874 |
GWAS Ctlg | rs1135401874 |
Max Magnitude | 0 |
aka NM_007294.3(BRCA1):c.4310delC or (p.Ser1437Leufs)
Pathogenic variant based on expert panel submission to ClinVar