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

rs587777060

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777060(C;T)
Make rs587777060(T;T)
ReferenceGRCh38 38.1/142
Chromosome21
Position42486428
GeneRSPH1
is asnp
is mentioned by
dbSNPrs587777060
ebirs587777060
HLIrs587777060
Exacrs587777060
Varsomers587777060
Maprs587777060
PheGenIrs587777060
hapmaprs587777060
1000 genomesrs587777060
hgdprs587777060
ensemblrs587777060
gopubmedrs587777060
geneviewrs587777060
scholarrs587777060
googlers587777060
pharmgkbrs587777060
gwascentralrs587777060
openSNPrs587777060
23andMers587777060
23andMe allrs587777060
SNP Nexus

SNPshotrs587777060
SNPdbers587777060
MSV3drs587777060
GWAS Ctlgrs587777060
Max Magnitude0
ClinVar
Risk rs587777060(T;T)
Alt rs587777060(T;T)
Reference rs587777060(C;C)
Significance Pathogenic
Disease Primary ciliary dyskinesia 24
Variation info
Gene RSPH1
CLNDBN Primary ciliary dyskinesia 24
Reversed 0
HGVS NC_000021.8:g.43906538C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000057513.3,