rs397508671
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CTCC;CTCC) | 0 | common in clinvar |
Make rs397508671(-;-) |
Make rs397508671(-;CTCC) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 117531034 |
Gene | CFTR |
is a | snp |
is | mentioned by |
dbSNP | rs397508671 |
dbSNP (classic) | rs397508671 |
ClinGen | rs397508671 |
ebi | rs397508671 |
HLI | rs397508671 |
Exac | rs397508671 |
Gnomad | rs397508671 |
Varsome | rs397508671 |
LitVar | rs397508671 |
Map | rs397508671 |
PheGenI | rs397508671 |
Biobank | rs397508671 |
1000 genomes | rs397508671 |
hgdp | rs397508671 |
ensembl | rs397508671 |
geneview | rs397508671 |
scholar | rs397508671 |
rs397508671 | |
pharmgkb | rs397508671 |
gwascentral | rs397508671 |
openSNP | rs397508671 |
23andMe | rs397508671 |
SNPshot | rs397508671 |
SNPdbe | rs397508671 |
MSV3d | rs397508671 |
GWAS Ctlg | rs397508671 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs397508671(-;-) |
Alt | rs397508671(-;-) |
Reference | Rs397508671(CTCC;CTCC) |
Significance | Untested |
Disease | Cystic fibrosis |
Variation | info |
Gene | CFTR |
CLNDBN | Cystic fibrosis |
Reversed | 0 |
HGVS | NC_000007.13:g.117171088_117171091delCTCC |
CLNSRC | ClinVar |
CLNACC | RCV000047071.2, |