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

rs587777059

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TACT;TACT) 0 common in clinvar
Make rs587777059(-;-)
Make rs587777059(-;TACT)
ReferenceGRCh38 38.1/142
Chromosome21
Position42485760
GeneRSPH1
is asnp
is mentioned by
dbSNPrs587777059
ebirs587777059
HLIrs587777059
Exacrs587777059
Varsomers587777059
Maprs587777059
PheGenIrs587777059
hapmaprs587777059
1000 genomesrs587777059
hgdprs587777059
ensemblrs587777059
gopubmedrs587777059
geneviewrs587777059
scholarrs587777059
googlers587777059
pharmgkbrs587777059
gwascentralrs587777059
openSNPrs587777059
23andMers587777059
23andMe allrs587777059
SNP Nexus

SNPshotrs587777059
SNPdbers587777059
MSV3drs587777059
GWAS Ctlgrs587777059
Max Magnitude0
ClinVar
Risk rs587777059(;)
Alt rs587777059(;)
Reference rs587777059(TACT;TACT)
Significance Pathogenic
Disease Primary ciliary dyskinesia 24 Kartagener syndrome
Variation info
Gene RSPH1
CLNDBN Primary ciliary dyskinesia 24 Kartagener syndrome
Reversed 0
HGVS NC_000021.8:g.43905870_43905873delTACT
CLNSRC OMIM Allelic Variant
CLNACC RCV000057511.3, RCV000190927.1,