rs121908689
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs121908689(A;A) |
Make rs121908689(A;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 46272758 |
Gene | RAD54L |
is a | snp |
is | mentioned by |
dbSNP | rs121908689 |
dbSNP (classic) | rs121908689 |
ClinGen | rs121908689 |
ebi | rs121908689 |
HLI | rs121908689 |
Exac | rs121908689 |
Gnomad | rs121908689 |
Varsome | rs121908689 |
LitVar | rs121908689 |
Map | rs121908689 |
PheGenI | rs121908689 |
Biobank | rs121908689 |
1000 genomes | rs121908689 |
hgdp | rs121908689 |
ensembl | rs121908689 |
geneview | rs121908689 |
scholar | rs121908689 |
rs121908689 | |
pharmgkb | rs121908689 |
gwascentral | rs121908689 |
openSNP | rs121908689 |
23andMe | rs121908689 |
SNPshot | rs121908689 |
SNPdbe | rs121908689 |
MSV3d | rs121908689 |
GWAS Ctlg | rs121908689 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs121908689(A;A) |
Alt | rs121908689(A;A) |
Reference | Rs121908689(T;T) |
Significance | Pathogenic |
Disease | Malignant lymphoma |
Variation | info |
Gene | RAD54L |
CLNDBN | Malignant lymphoma, non-Hodgkin |
Reversed | 0 |
HGVS | NC_000001.10:g.46738430T>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000006569.4, |