rs1860545
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1860545(C;C) |
Make rs1860545(C;T) |
Make rs1860545(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 6337611 |
Gene | TNFRSF1A |
is a | snp |
is | mentioned by |
dbSNP | rs1860545 |
dbSNP (classic) | rs1860545 |
ClinGen | rs1860545 |
ebi | rs1860545 |
HLI | rs1860545 |
Exac | rs1860545 |
Gnomad | rs1860545 |
Varsome | rs1860545 |
LitVar | rs1860545 |
Map | rs1860545 |
PheGenI | rs1860545 |
Biobank | rs1860545 |
1000 genomes | rs1860545 |
hgdp | rs1860545 |
ensembl | rs1860545 |
geneview | rs1860545 |
scholar | rs1860545 |
rs1860545 | |
pharmgkb | rs1860545 |
gwascentral | rs1860545 |
openSNP | rs1860545 |
23andMe | rs1860545 |
SNPshot | rs1860545 |
SNPdbe | rs1860545 |
MSV3d | rs1860545 |
GWAS Ctlg | rs1860545 |
GMAF | 0.2475 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 20430450] Validation of the CD6 and TNFRSF1A loci as risk factors for multiple sclerosis in Spain
[PMID 18520591] Sequence variants in host cell factor C1 are associated with Meniere's disease.