rs397508658
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;T) | 3 | carrier of a cystic fibrosis allele |
(T;T) | 0 | common/normal |
Make rs397508658(C;C) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 7 |
Position | 117664728 |
Gene | CFTR |
is a | snp |
is | mentioned by |
dbSNP | rs397508658 |
dbSNP (classic) | rs397508658 |
ClinGen | rs397508658 |
ebi | rs397508658 |
HLI | rs397508658 |
Exac | rs397508658 |
Gnomad | rs397508658 |
Varsome | rs397508658 |
LitVar | rs397508658 |
Map | rs397508658 |
PheGenI | rs397508658 |
Biobank | rs397508658 |
1000 genomes | rs397508658 |
hgdp | rs397508658 |
ensembl | rs397508658 |
geneview | rs397508658 |
scholar | rs397508658 |
rs397508658 | |
pharmgkb | rs397508658 |
gwascentral | rs397508658 |
openSNP | rs397508658 |
23andMe | rs397508658 |
SNPshot | rs397508658 |
SNPdbe | rs397508658 |
MSV3d | rs397508658 |
GWAS Ctlg | rs397508658 |
Max Magnitude | 3 |