rs369419645
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs369419645(C;T) |
Make rs369419645(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 20 |
Position | 63688312 |
Gene | RTEL1, RTEL1-TNFRSF6B |
is a | snp |
is | mentioned by |
dbSNP | rs369419645 |
dbSNP (classic) | rs369419645 |
ClinGen | rs369419645 |
ebi | rs369419645 |
HLI | rs369419645 |
Exac | rs369419645 |
Gnomad | rs369419645 |
Varsome | rs369419645 |
LitVar | rs369419645 |
Map | rs369419645 |
PheGenI | rs369419645 |
Biobank | rs369419645 |
1000 genomes | rs369419645 |
hgdp | rs369419645 |
ensembl | rs369419645 |
geneview | rs369419645 |
scholar | rs369419645 |
rs369419645 | |
pharmgkb | rs369419645 |
gwascentral | rs369419645 |
openSNP | rs369419645 |
23andMe | rs369419645 |
SNPshot | rs369419645 |
SNPdbe | rs369419645 |
MSV3d | rs369419645 |
GWAS Ctlg | rs369419645 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs369419645(T;T) |
Alt | rs369419645(T;T) |
Reference | Rs369419645(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | RTEL1-TNFRSF6B RTEL1 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000020.10:g.62319665C>T |
CLNSRC | |
CLNACC | RCV000478358.1, |