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rs587776910

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs587776910(-;-)
Make rs587776910(-;G)
Make rs587776910(G;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position44902471
GeneCCDC103
is asnp
is mentioned by
dbSNPrs587776910
ebirs587776910
HLIrs587776910
Exacrs587776910
Varsomers587776910
Maprs587776910
PheGenIrs587776910
hapmaprs587776910
1000 genomesrs587776910
hgdprs587776910
ensemblrs587776910
gopubmedrs587776910
geneviewrs587776910
scholarrs587776910
googlers587776910
pharmgkbrs587776910
gwascentralrs587776910
openSNPrs587776910
23andMers587776910
23andMe allrs587776910
SNP Nexus

SNPshotrs587776910
SNPdbers587776910
MSV3drs587776910
GWAS Ctlgrs587776910
Max Magnitude0
ClinVar
Risk rs587776910(G;G)
Alt rs587776910(G;G)
Reference rs587776910(;)
Significance Pathogenic
Disease Ciliary dyskinesia Kartagener syndrome
Variation info
Gene CCDC103
CLNDBN Ciliary dyskinesia, primary, 17 Kartagener syndrome
Reversed 0
HGVS NC_000017.10:g.42979839dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000024375.3, RCV000190915.1,