rs1135401914
From SNPedia
Orientation | plus |
Make rs1135401914(-;-) |
Make rs1135401914(-;A) |
Make rs1135401914(A;A) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 13 |
Position | 32340846 |
Gene | BRCA2 |
is a | snp |
is | mentioned by |
dbSNP | rs1135401914 |
dbSNP (classic) | rs1135401914 |
ClinGen | rs1135401914 |
ebi | rs1135401914 |
HLI | rs1135401914 |
Exac | rs1135401914 |
Gnomad | rs1135401914 |
Varsome | rs1135401914 |
LitVar | rs1135401914 |
Map | rs1135401914 |
PheGenI | rs1135401914 |
Biobank | rs1135401914 |
1000 genomes | rs1135401914 |
hgdp | rs1135401914 |
ensembl | rs1135401914 |
geneview | rs1135401914 |
scholar | rs1135401914 |
rs1135401914 | |
pharmgkb | rs1135401914 |
gwascentral | rs1135401914 |
openSNP | rs1135401914 |
23andMe | rs1135401914 |
SNPshot | rs1135401914 |
SNPdbe | rs1135401914 |
MSV3d | rs1135401914 |
GWAS Ctlg | rs1135401914 |
Max Magnitude | 0 |
aka NM_000059.3(BRCA2):c.6491delA or (p.Gln2164Argfs)
Pathogenic variant based on expert panel submission to ClinVar