rs16994592
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in complete genomics |
Make rs16994592(C;C) |
Make rs16994592(C;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 19 |
Position | 6586487 |
Gene | CD70 |
is a | snp |
is | mentioned by |
dbSNP | rs16994592 |
dbSNP (classic) | rs16994592 |
ClinGen | rs16994592 |
ebi | rs16994592 |
HLI | rs16994592 |
Exac | rs16994592 |
Gnomad | rs16994592 |
Varsome | rs16994592 |
LitVar | rs16994592 |
Map | rs16994592 |
PheGenI | rs16994592 |
Biobank | rs16994592 |
1000 genomes | rs16994592 |
hgdp | rs16994592 |
ensembl | rs16994592 |
geneview | rs16994592 |
scholar | rs16994592 |
rs16994592 | |
pharmgkb | rs16994592 |
gwascentral | rs16994592 |
openSNP | rs16994592 |
23andMe | rs16994592 |
SNPshot | rs16994592 |
SNPdbe | rs16994592 |
MSV3d | rs16994592 |
GWAS Ctlg | rs16994592 |
GMAF | 0.08448 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
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[PMID 19390683] Common Gene Variants in the Tumor Necrosis Factor (TNF) and TNF Receptor Superfamilies and NF-kB Transcription Factors and Non-Hodgkin Lymphoma Risk