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

rs587777045

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CA;CA) 0 common in clinvar
Make rs587777045(-;-)
Make rs587777045(-;CA)
ReferenceGRCh38 38.1/142
Chromosome3
Position50343123
GeneZMYND10
is asnp
is mentioned by
dbSNPrs587777045
dbSNP (classic)rs587777045
ClinGenrs587777045
ebirs587777045
HLIrs587777045
Exacrs587777045
Gnomadrs587777045
Varsomers587777045
LitVarrs587777045
Maprs587777045
PheGenIrs587777045
Biobankrs587777045
1000 genomesrs587777045
hgdprs587777045
ensemblrs587777045
geneviewrs587777045
scholarrs587777045
googlers587777045
pharmgkbrs587777045
gwascentralrs587777045
openSNPrs587777045
23andMers587777045
SNPshotrs587777045
SNPdbers587777045
MSV3drs587777045
GWAS Ctlgrs587777045
Max Magnitude0
ClinVar
Risk rs587777045(-;-)
Alt rs587777045(-;-)
Reference Rs587777045(CA;CA)
Significance Pathogenic
Disease Ciliary dyskinesia
Variation info
Gene ZMYND10
CLNDBN Ciliary dyskinesia, primary, 22
Reversed 0
HGVS NC_000003.11:g.50380554_50380555delCA
CLNSRC OMIM Allelic Variant
CLNACC RCV000056268.3,