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rs779506456

From SNPedia

Orientationplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs779506456(-;A)
Make rs779506456(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position13829618
GeneDNAH5
is asnp
is mentioned by
dbSNPrs779506456
ClinGenrs779506456
ebirs779506456
HLIrs779506456
Exacrs779506456
Varsomers779506456
Maprs779506456
PheGenIrs779506456
hapmaprs779506456
1000 genomesrs779506456
hgdprs779506456
ensemblrs779506456
gopubmedrs779506456
geneviewrs779506456
scholarrs779506456
googlers779506456
pharmgkbrs779506456
gwascentralrs779506456
openSNPrs779506456
23andMers779506456
23andMe allrs779506456
SNP Nexus

SNPshotrs779506456
SNPdbers779506456
MSV3drs779506456
GWAS Ctlgrs779506456
Max Magnitude0
ClinVar
Risk rs779506456(A;A)
Alt rs779506456(A;A)
Reference Rs779506456(;)
Significance Pathogenic
Disease Primary ciliary dyskinesia
Variation info
Gene DNAH5
CLNDBN Primary ciliary dyskinesia
Reversed 0
HGVS NC_000005.9:g.13829727_13829728insA
CLNSRC
CLNACC RCV000206107.1,