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rs79967166

From SNPedia

Orientationminus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs79967166(C;C)
Make rs79967166(C;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position13754203
GeneDNAH5
is asnp
is mentioned by
dbSNPrs79967166
ebirs79967166
HLIrs79967166
Exacrs79967166
Varsomers79967166
Maprs79967166
PheGenIrs79967166
hapmaprs79967166
1000 genomesrs79967166
hgdprs79967166
ensemblrs79967166
gopubmedrs79967166
geneviewrs79967166
scholarrs79967166
googlers79967166
pharmgkbrs79967166
gwascentralrs79967166
openSNPrs79967166
23andMers79967166
23andMe allrs79967166
SNP Nexus

SNPshotrs79967166
SNPdbers79967166
MSV3drs79967166
GWAS Ctlgrs79967166
Max Magnitude0
OMIM603335
Desc
Variant0002
Relatedalso
ClinVar
Risk rs79967166(C;C)
Alt rs79967166(C;C)
Reference rs79967166(G;G)
Significance Pathogenic
Disease Ciliary dyskinesia
Variation info
Gene DNAH5
CLNDBN Ciliary dyskinesia, primary, 3
Reversed 1
HGVS NC_000005.9:g.13754312C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006851.2,