rs1135401864
From SNPedia
Orientation | minus |
Make rs1135401864(G;G) |
Make rs1135401864(G;T) |
Make rs1135401864(T;T) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 17 |
Position | 43091894 |
Gene | BRCA1 |
is a | snp |
is | mentioned by |
dbSNP | rs1135401864 |
dbSNP (classic) | rs1135401864 |
ClinGen | rs1135401864 |
ebi | rs1135401864 |
HLI | rs1135401864 |
Exac | rs1135401864 |
Gnomad | rs1135401864 |
Varsome | rs1135401864 |
LitVar | rs1135401864 |
Map | rs1135401864 |
PheGenI | rs1135401864 |
Biobank | rs1135401864 |
1000 genomes | rs1135401864 |
hgdp | rs1135401864 |
ensembl | rs1135401864 |
geneview | rs1135401864 |
scholar | rs1135401864 |
rs1135401864 | |
pharmgkb | rs1135401864 |
gwascentral | rs1135401864 |
openSNP | rs1135401864 |
23andMe | rs1135401864 |
SNPshot | rs1135401864 |
SNPdbe | rs1135401864 |
MSV3d | rs1135401864 |
GWAS Ctlg | rs1135401864 |
Max Magnitude | 0 |
aka NM_007294.3(BRCA1):c.3637G>T or (p.Glu1213Ter)
Pathogenic variant based on expert panel submission to ClinVar