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

rs863224503

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224503(A;C)
Make rs863224503(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position13708337
GeneDNAH5
is asnp
is mentioned by
dbSNPrs863224503
ebirs863224503
HLIrs863224503
Exacrs863224503
Varsomers863224503
Maprs863224503
PheGenIrs863224503
hapmaprs863224503
1000 genomesrs863224503
hgdprs863224503
ensemblrs863224503
gopubmedrs863224503
geneviewrs863224503
scholarrs863224503
googlers863224503
pharmgkbrs863224503
gwascentralrs863224503
openSNPrs863224503
23andMers863224503
23andMe allrs863224503
SNP Nexus

SNPshotrs863224503
SNPdbers863224503
MSV3drs863224503
GWAS Ctlgrs863224503
Max Magnitude0
ClinVar
Risk rs863224503(C;C)
Alt rs863224503(C;C)
Reference rs863224503(A;A)
Significance Pathogenic
Disease Primary ciliary dyskinesia
Variation info
Gene DNAH5
CLNDBN Primary ciliary dyskinesia
Reversed 1
HGVS NC_000005.9:g.13708446T>G
CLNSRC
CLNACC RCV000197324.1,