rs121908810
From SNPedia
Cystic Fibrosis related |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 3 | cystic fibrosis carrier |
Make rs121908810(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 117592457 |
Gene | CFTR |
is a | snp |
is | mentioned by |
dbSNP | rs121908810 |
dbSNP (classic) | rs121908810 |
ClinGen | rs121908810 |
ebi | rs121908810 |
HLI | rs121908810 |
Exac | rs121908810 |
Gnomad | rs121908810 |
Varsome | rs121908810 |
LitVar | rs121908810 |
Map | rs121908810 |
PheGenI | rs121908810 |
Biobank | rs121908810 |
1000 genomes | rs121908810 |
hgdp | rs121908810 |
ensembl | rs121908810 |
geneview | rs121908810 |
scholar | rs121908810 |
rs121908810 | |
pharmgkb | rs121908810 |
gwascentral | rs121908810 |
openSNP | rs121908810 |
23andMe | rs121908810 |
SNPshot | rs121908810 |
SNPdbe | rs121908810 |
MSV3d | rs121908810 |
GWAS Ctlg | rs121908810 |
Max Magnitude | 3 |
Cystic fibrosis; c.2290C>T, p.Arg764Ter
named i5011532 by 23andMe
ClinVar | |
---|---|
Risk | rs121908810(T;T) |
Alt | rs121908810(T;T) |
Reference | Rs121908810(C;C) |
Significance | Pathogenic |
Disease | Cystic fibrosis |
Variation | info |
Gene | CFTR |
CLNDBN | Cystic fibrosis |
Reversed | 0 |
HGVS | NC_000007.13:g.117232511C>T |
CLNSRC | CFTR2 |
CLNACC | RCV000056363.3, |