rs797045146
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
(I;I) | 0 | common genotype |
Make rs797045146(-;-) |
Make rs797045146(-;G) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 14 |
Position | 49635119 |
Gene | DNAAF2 |
is a | snp |
is | mentioned by |
dbSNP | rs797045146 |
dbSNP (classic) | rs797045146 |
ClinGen | rs797045146 |
ebi | rs797045146 |
HLI | rs797045146 |
Exac | rs797045146 |
Gnomad | rs797045146 |
Varsome | rs797045146 |
LitVar | rs797045146 |
Map | rs797045146 |
PheGenI | rs797045146 |
Biobank | rs797045146 |
1000 genomes | rs797045146 |
hgdp | rs797045146 |
ensembl | rs797045146 |
geneview | rs797045146 |
scholar | rs797045146 |
rs797045146 | |
pharmgkb | rs797045146 |
gwascentral | rs797045146 |
openSNP | rs797045146 |
23andMe | rs797045146 |
SNPshot | rs797045146 |
SNPdbe | rs797045146 |
MSV3d | rs797045146 |
GWAS Ctlg | rs797045146 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797045146(-;-) |
Alt | rs797045146(-;-) |
Reference | Rs797045146(G;G) |
Significance | Pathogenic |
Disease | Kartagener syndrome |
Variation | info |
Gene | DNAAF2 |
CLNDBN | Kartagener syndrome |
Reversed | 1 |
HGVS | NC_000014.8:g.50101837delC |
CLNSRC | |
CLNACC | RCV000190911.1, |