rs397508169
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(ACGACTA;ACGACTA) | 0 | common in clinvar |
(TAACGAC;TAACGAC) | 0 | common in clinvar |
Make rs397508169(-;-) |
Make rs397508169(-;ACGACTA) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 117542061 |
Gene | CFTR |
is a | snp |
is | mentioned by |
dbSNP | rs397508169 |
dbSNP (classic) | rs397508169 |
ClinGen | rs397508169 |
ebi | rs397508169 |
HLI | rs397508169 |
Exac | rs397508169 |
Gnomad | rs397508169 |
Varsome | rs397508169 |
LitVar | rs397508169 |
Map | rs397508169 |
PheGenI | rs397508169 |
Biobank | rs397508169 |
1000 genomes | rs397508169 |
hgdp | rs397508169 |
ensembl | rs397508169 |
geneview | rs397508169 |
scholar | rs397508169 |
rs397508169 | |
pharmgkb | rs397508169 |
gwascentral | rs397508169 |
openSNP | rs397508169 |
23andMe | rs397508169 |
SNPshot | rs397508169 |
SNPdbe | rs397508169 |
MSV3d | rs397508169 |
GWAS Ctlg | rs397508169 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397508169(-;-) |
Alt | rs397508169(-;-) |
Reference | Rs397508169(TAACGAC;TAACGAC) |
Significance | Untested |
Disease | Cystic fibrosis |
Variation | info |
Gene | CFTR |
CLNDBN | Cystic fibrosis |
Reversed | 0 |
HGVS | NC_000007.13:g.117182115_117182121delACGACTA |
CLNSRC | ClinVar |
CLNACC | RCV000046249.2, |