Have questions? Visit https://www.reddit.com/r/SNPedia

rs587777501

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
(G;G) 0 common in clinvar
Make rs587777501(A;A)
Make rs587777501(A;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position55231467
GeneCCNO
is asnp
is mentioned by
dbSNPrs587777501
ebirs587777501
HLIrs587777501
Exacrs587777501
Varsomers587777501
Maprs587777501
PheGenIrs587777501
hapmaprs587777501
1000 genomesrs587777501
hgdprs587777501
ensemblrs587777501
gopubmedrs587777501
geneviewrs587777501
scholarrs587777501
googlers587777501
pharmgkbrs587777501
gwascentralrs587777501
openSNPrs587777501
23andMers587777501
23andMe allrs587777501
SNP Nexus

SNPshotrs587777501
SNPdbers587777501
MSV3drs587777501
GWAS Ctlgrs587777501
Max Magnitude0
ClinVar
Risk rs587777501(A,G;A,G)
Alt rs587777501(A,G;A,G)
Reference rs587777501(C;C)
Significance Pathogenic
Disease Ciliary dyskinesia Kartagener syndrome
Variation info
Gene CCNO
CLNDBN Ciliary dyskinesia, primary, 29 Kartagener syndrome
Reversed 1
HGVS NC_000005.9:g.54527295G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000128543.3, RCV000190947.1,