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rs863224504

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs863224504(C;T)
Make rs863224504(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position13770852
GeneDNAH5
is asnp
is mentioned by
dbSNPrs863224504
ebirs863224504
HLIrs863224504
Exacrs863224504
Varsomers863224504
Maprs863224504
PheGenIrs863224504
hapmaprs863224504
1000 genomesrs863224504
hgdprs863224504
ensemblrs863224504
gopubmedrs863224504
geneviewrs863224504
scholarrs863224504
googlers863224504
pharmgkbrs863224504
gwascentralrs863224504
openSNPrs863224504
23andMers863224504
23andMe allrs863224504
SNP Nexus

SNPshotrs863224504
SNPdbers863224504
MSV3drs863224504
GWAS Ctlgrs863224504
Max Magnitude0
ClinVar
Risk rs863224504(T;T)
Alt rs863224504(T;T)
Reference rs863224504(C;C)
Significance Pathogenic
Disease Primary ciliary dyskinesia
Variation info
Gene DNAH5
CLNDBN Primary ciliary dyskinesia
Reversed 1
HGVS NC_000005.9:g.13770961G>A
CLNSRC
CLNACC RCV000198869.1,