rs397508473
From SNPedia
Merged into | rs397508472 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AATT;AATT) | 0 | common in clinvar |
(ATTA;ATTA) | 0 | common in clinvar |
Make rs397508473(-;-) |
Make rs397508473(-;AATT) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 117610527 |
Gene | CFTR |
is a | snp |
is | mentioned by |
dbSNP | rs397508473 |
dbSNP (classic) | rs397508473 |
ClinGen | rs397508473 |
ebi | rs397508473 |
HLI | rs397508473 |
Exac | rs397508473 |
Gnomad | rs397508473 |
Varsome | rs397508473 |
LitVar | rs397508473 |
Map | rs397508473 |
PheGenI | rs397508473 |
Biobank | rs397508473 |
1000 genomes | rs397508473 |
hgdp | rs397508473 |
ensembl | rs397508473 |
geneview | rs397508473 |
scholar | rs397508473 |
rs397508473 | |
pharmgkb | rs397508473 |
gwascentral | rs397508473 |
openSNP | rs397508473 |
23andMe | rs397508473 |
SNPshot | rs397508473 |
SNPdbe | rs397508473 |
MSV3d | rs397508473 |
GWAS Ctlg | rs397508473 |
Status | Merged into rs397508472 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs397508473(ATTA;ATTA) |
Significance | Untested |
Disease | Cystic fibrosis |
Variation | info |
Gene | CFTR |
CLNDBN | Cystic fibrosis |
Reversed | 0 |
HGVS | NC_000007.13:g.117250581_117250584delAATT |
CLNSRC | ClinVar |
CLNACC | RCV000046747.4, |