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rs587777779

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777779(A;A)
Make rs587777779(A;C)
ReferenceGRCh38 38.1/142
Chromosome19
Position11426182
GeneCCDC151
is asnp
is mentioned by
dbSNPrs587777779
ebirs587777779
HLIrs587777779
Exacrs587777779
Varsomers587777779
Maprs587777779
PheGenIrs587777779
hapmaprs587777779
1000 genomesrs587777779
hgdprs587777779
ensemblrs587777779
gopubmedrs587777779
geneviewrs587777779
scholarrs587777779
googlers587777779
pharmgkbrs587777779
gwascentralrs587777779
openSNPrs587777779
23andMers587777779
23andMe allrs587777779
SNP Nexus

SNPshotrs587777779
SNPdbers587777779
MSV3drs587777779
GWAS Ctlgrs587777779
Max Magnitude0
ClinVar
Risk rs587777779(A;A)
Alt rs587777779(A;A)
Reference rs587777779(C;C)
Significance Pathogenic
Disease Ciliary dyskinesia Kartagener syndrome
Variation info
Gene CCDC151
CLNDBN Ciliary dyskinesia, primary, 30 Kartagener syndrome
Reversed 0
HGVS NC_000019.9:g.11537002C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000144449.3, RCV000190932.1,