rs104895245
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs104895245(C;C) |
Make rs104895245(C;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 12 |
Position | 6333794 |
Gene | TNFRSF1A |
is a | snp |
is | mentioned by |
dbSNP | rs104895245 |
dbSNP (classic) | rs104895245 |
ClinGen | rs104895245 |
ebi | rs104895245 |
HLI | rs104895245 |
Exac | rs104895245 |
Gnomad | rs104895245 |
Varsome | rs104895245 |
LitVar | rs104895245 |
Map | rs104895245 |
PheGenI | rs104895245 |
Biobank | rs104895245 |
1000 genomes | rs104895245 |
hgdp | rs104895245 |
ensembl | rs104895245 |
geneview | rs104895245 |
scholar | rs104895245 |
rs104895245 | |
pharmgkb | rs104895245 |
gwascentral | rs104895245 |
openSNP | rs104895245 |
23andMe | rs104895245 |
SNPshot | rs104895245 |
SNPdbe | rs104895245 |
MSV3d | rs104895245 |
GWAS Ctlg | rs104895245 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs104895245(C;C) rs104895245(G;G) |
Alt | rs104895245(C;C) rs104895245(G;G) |
Reference | Rs104895245(T;T) |
Significance | Probable-Pathogenic |
Disease | TNF receptor-associated periodic fever syndrome (TRAPS) not provided |
Variation | info |
Gene | TNFRSF1A |
CLNDBN | TNF receptor-associated periodic fever syndrome (TRAPS) not provided |
Reversed | 1 |
HGVS | NC_000012.11:g.6442960A>C; NC_000012.11:g.6442960A>G |
CLNSRC | |
CLNACC | RCV000083930.1, RCV000083929.1, RCV000254771.1, |