rs139805921
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs139805921(A;A) |
Make rs139805921(A;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 21 |
Position | 42388935 |
Gene | TMPRSS3 |
is a | snp |
is | mentioned by |
dbSNP | rs139805921 |
dbSNP (classic) | rs139805921 |
ClinGen | rs139805921 |
ebi | rs139805921 |
HLI | rs139805921 |
Exac | rs139805921 |
Gnomad | rs139805921 |
Varsome | rs139805921 |
LitVar | rs139805921 |
Map | rs139805921 |
PheGenI | rs139805921 |
Biobank | rs139805921 |
1000 genomes | rs139805921 |
hgdp | rs139805921 |
ensembl | rs139805921 |
geneview | rs139805921 |
scholar | rs139805921 |
rs139805921 | |
pharmgkb | rs139805921 |
gwascentral | rs139805921 |
openSNP | rs139805921 |
23andMe | rs139805921 |
SNPshot | rs139805921 |
SNPdbe | rs139805921 |
MSV3d | rs139805921 |
GWAS Ctlg | rs139805921 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs139805921(A;A) |
Alt | rs139805921(A;A) |
Reference | Rs139805921(G;G) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | TMPRSS3 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000021.8:g.43809044G>A |
CLNSRC | |
CLNACC | RCV000441150.1, |