rs148173473
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs148173473(A;G) |
Make rs148173473(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 7 |
Position | 117587760 |
Gene | CFTR |
is a | snp |
is | mentioned by |
dbSNP | rs148173473 |
dbSNP (classic) | rs148173473 |
ClinGen | rs148173473 |
ebi | rs148173473 |
HLI | rs148173473 |
Exac | rs148173473 |
Gnomad | rs148173473 |
Varsome | rs148173473 |
LitVar | rs148173473 |
Map | rs148173473 |
PheGenI | rs148173473 |
Biobank | rs148173473 |
1000 genomes | rs148173473 |
hgdp | rs148173473 |
ensembl | rs148173473 |
geneview | rs148173473 |
scholar | rs148173473 |
rs148173473 | |
pharmgkb | rs148173473 |
gwascentral | rs148173473 |
openSNP | rs148173473 |
23andMe | rs148173473 |
SNPshot | rs148173473 |
SNPdbe | rs148173473 |
MSV3d | rs148173473 |
GWAS Ctlg | rs148173473 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs148173473(G;G) rs148173473(T;T) |
Alt | rs148173473(G;G) rs148173473(T;T) |
Reference | Rs148173473(A;A) |
Significance | Untested |
Disease | Cystic fibrosis |
Variation | info |
Gene | CFTR |
CLNDBN | Cystic fibrosis |
Reversed | 0 |
HGVS | NC_000007.13:g.117227814A>T |
CLNSRC | ClinVar |
CLNACC | RCV000046360.2, |