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rs587777502

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
(T;T) 0 common in clinvar
Make rs587777502(-;-)
Make rs587777502(-;GGGCT)
Make rs587777502(GGGCT;GGGCT)
ReferenceGRCh38 38.1/142
Chromosome5
Position55233261
GeneCCNO
is asnp
is mentioned by
dbSNPrs587777502
ebirs587777502
HLIrs587777502
Exacrs587777502
Varsomers587777502
Maprs587777502
PheGenIrs587777502
hapmaprs587777502
1000 genomesrs587777502
hgdprs587777502
ensemblrs587777502
gopubmedrs587777502
geneviewrs587777502
scholarrs587777502
googlers587777502
pharmgkbrs587777502
gwascentralrs587777502
openSNPrs587777502
23andMers587777502
23andMe allrs587777502
SNP Nexus

SNPshotrs587777502
SNPdbers587777502
MSV3drs587777502
GWAS Ctlgrs587777502
Max Magnitude0
ClinVar
Risk rs587777502(TGGGCC,TGGGCT;TGGGCC,TGGGCT)
Alt rs587777502(TGGGCC,TGGGCT;TGGGCC,TGGGCT)
Reference rs587777502(T;T)
Significance Pathogenic
Disease Ciliary dyskinesia Kartagener syndrome
Variation info
Gene CCNO
CLNDBN Ciliary dyskinesia, primary, 29 Kartagener syndrome
Reversed 0
HGVS NC_000005.9:g.54529085_54529089dupGGGCT
CLNSRC OMIM Allelic Variant
CLNACC RCV000128544.3, RCV000190943.1,