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rs587777500

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777500(-;-)
Make rs587777500(-;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position55231502
GeneCCNO
is asnp
is mentioned by
dbSNPrs587777500
ebirs587777500
HLIrs587777500
Exacrs587777500
Varsomers587777500
Maprs587777500
PheGenIrs587777500
hapmaprs587777500
1000 genomesrs587777500
hgdprs587777500
ensemblrs587777500
gopubmedrs587777500
geneviewrs587777500
scholarrs587777500
googlers587777500
pharmgkbrs587777500
gwascentralrs587777500
openSNPrs587777500
23andMers587777500
23andMe allrs587777500
SNP Nexus

SNPshotrs587777500
SNPdbers587777500
MSV3drs587777500
GWAS Ctlgrs587777500
Max Magnitude0
ClinVar
Risk rs587777500(GG,G;GG,G)
Alt rs587777500(GG,G;GG,G)
Reference rs587777500(CG;CG)
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.54527330delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000128542.3, RCV000190946.1,