rs606231164
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
(-;AATA) | 3 | Carrier of a primary ciliary dyskinesia mutation |
Make rs606231164(AATA;AATA) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 9 |
Position | 34489343 |
Gene | DNAI1 |
is a | snp |
is | mentioned by |
dbSNP | rs606231164 |
dbSNP (classic) | rs606231164 |
ClinGen | rs606231164 |
ebi | rs606231164 |
HLI | rs606231164 |
Exac | rs606231164 |
Gnomad | rs606231164 |
Varsome | rs606231164 |
LitVar | rs606231164 |
Map | rs606231164 |
PheGenI | rs606231164 |
Biobank | rs606231164 |
1000 genomes | rs606231164 |
hgdp | rs606231164 |
ensembl | rs606231164 |
geneview | rs606231164 |
scholar | rs606231164 |
rs606231164 | |
pharmgkb | rs606231164 |
gwascentral | rs606231164 |
openSNP | rs606231164 |
23andMe | rs606231164 |
SNPshot | rs606231164 |
SNPdbe | rs606231164 |
MSV3d | rs606231164 |
GWAS Ctlg | rs606231164 |
Max Magnitude | 3 |
aka c.282_283insAATA (p.Gly95Asnfs)
ClinVar | |
---|---|
Risk | rs606231164(AATA;AATA) |
Alt | rs606231164(AATA;AATA) |
Reference | Rs606231164(-;-) |
Significance | Pathogenic |
Disease | Kartagener syndrome |
Variation | info |
Gene | DNAI1 |
CLNDBN | Kartagener syndrome |
Reversed | 0 |
HGVS | NC_000009.11:g.34489341_34489342insAATA |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000005955.4, |