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

rs878855279

From SNPedia

Orientationminus
Geno Mag Summary
(CAAA;CAAA) 0 common in clinvar
Make rs878855279(-;-)
Make rs878855279(-;CAAA)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position180651492
GeneCCDC39
is asnp
is mentioned by
dbSNPrs878855279
ebirs878855279
HLIrs878855279
Exacrs878855279
Varsomers878855279
Maprs878855279
PheGenIrs878855279
hapmaprs878855279
1000 genomesrs878855279
hgdprs878855279
ensemblrs878855279
gopubmedrs878855279
geneviewrs878855279
scholarrs878855279
googlers878855279
pharmgkbrs878855279
gwascentralrs878855279
openSNPrs878855279
23andMers878855279
23andMe allrs878855279
SNP Nexus

SNPshotrs878855279
SNPdbers878855279
MSV3drs878855279
GWAS Ctlgrs878855279
Max Magnitude0
ClinVar
Risk rs878855279(;)
Alt rs878855279(;)
Reference rs878855279(CAAA;CAAA)
Significance Pathogenic
Disease Primary ciliary dyskinesia
Variation info
Gene CCDC39
CLNDBN Primary ciliary dyskinesia
Reversed 1
HGVS NC_000003.11:g.180369280_180369283delTTTG
CLNSRC
CLNACC RCV000232422.1,