rs35896902
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs35896902(C;C) |
Make rs35896902(C;T) |
Make rs35896902(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 1 |
Position | 182581355 |
Gene | RNASEL |
is a | snp |
is | mentioned by |
dbSNP | rs35896902 |
dbSNP (classic) | rs35896902 |
ClinGen | rs35896902 |
ebi | rs35896902 |
HLI | rs35896902 |
Exac | rs35896902 |
Gnomad | rs35896902 |
Varsome | rs35896902 |
LitVar | rs35896902 |
Map | rs35896902 |
PheGenI | rs35896902 |
Biobank | rs35896902 |
1000 genomes | rs35896902 |
hgdp | rs35896902 |
ensembl | rs35896902 |
geneview | rs35896902 |
scholar | rs35896902 |
rs35896902 | |
pharmgkb | rs35896902 |
gwascentral | rs35896902 |
openSNP | rs35896902 |
23andMe | rs35896902 |
SNPshot | rs35896902 |
SNPdbe | rs35896902 |
MSV3d | rs35896902 |
GWAS Ctlg | rs35896902 |
Max Magnitude | 0 |
[PMID 26236721] Functional and Structural Consequences of Damaging Single Nucleotide Polymorphisms in Human Prostate Cancer Predisposition Gene RNASEL.