rs139484231
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs139484231(C;T) |
Make rs139484231(T;T) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 21 |
Position | 42388523 |
Gene | TMPRSS3 |
is a | snp |
is | mentioned by |
dbSNP | rs139484231 |
dbSNP (classic) | rs139484231 |
ClinGen | rs139484231 |
ebi | rs139484231 |
HLI | rs139484231 |
Exac | rs139484231 |
Gnomad | rs139484231 |
Varsome | rs139484231 |
LitVar | rs139484231 |
Map | rs139484231 |
PheGenI | rs139484231 |
Biobank | rs139484231 |
1000 genomes | rs139484231 |
hgdp | rs139484231 |
ensembl | rs139484231 |
geneview | rs139484231 |
scholar | rs139484231 |
rs139484231 | |
pharmgkb | rs139484231 |
gwascentral | rs139484231 |
openSNP | rs139484231 |
23andMe | rs139484231 |
SNPshot | rs139484231 |
SNPdbe | rs139484231 |
MSV3d | rs139484231 |
GWAS Ctlg | rs139484231 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs139484231(T;T) |
Alt | rs139484231(T;T) |
Reference | Rs139484231(C;C) |
Significance | Probable-Pathogenic |
Disease | not specified not provided |
Variation | info |
Gene | TMPRSS3 |
CLNDBN | not specified not provided |
Reversed | 0 |
HGVS | NC_000021.8:g.43808632C>T |
CLNSRC | |
CLNACC | RCV000178994.1, RCV000493533.1, |