rs139304906
From SNPedia
Cystic Fibrosis related |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;T) | 3 | cystic fibrosis carrier |
(T;T) | 0 | common in clinvar |
Make rs139304906(C;C) |
Chromosome | 7 |
Position | 117611671 |
Gene | CFTR |
is a | snp |
is | mentioned by |
dbSNP | rs139304906 |
dbSNP (classic) | rs139304906 |
ClinGen | rs139304906 |
ebi | rs139304906 |
HLI | rs139304906 |
Exac | rs139304906 |
Gnomad | rs139304906 |
Varsome | rs139304906 |
LitVar | rs139304906 |
Map | rs139304906 |
PheGenI | rs139304906 |
Biobank | rs139304906 |
1000 genomes | rs139304906 |
hgdp | rs139304906 |
ensembl | rs139304906 |
geneview | rs139304906 |
scholar | rs139304906 |
rs139304906 | |
pharmgkb | rs139304906 |
gwascentral | rs139304906 |
openSNP | rs139304906 |
23andMe | rs139304906 |
SNPshot | rs139304906 |
SNPdbe | rs139304906 |
MSV3d | rs139304906 |
GWAS Ctlg | rs139304906 |
Max Magnitude | 3 |
Cystic fibrosis; c.3230T>C, p.Leu1077Pro
named i5011836 by 23andMe
ClinVar | |
---|---|
Risk | rs139304906(C;C) |
Alt | rs139304906(C;C) |
Reference | Rs139304906(T;T) |
Significance | Pathogenic |
Disease | Cystic fibrosis |
Variation | info |
Gene | CFTR |
CLNDBN | Cystic fibrosis |
Reversed | 0 |
HGVS | NC_000007.13:g.117251725T>C |
CLNSRC | UniProtKB (protein) |
CLNACC | RCV000056377.3, |