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rs373946181

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs373946181(C;T)
Make rs373946181(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position21705497
GeneDNAH11
is asnp
is mentioned by
dbSNPrs373946181
ebirs373946181
HLIrs373946181
Exacrs373946181
Varsomers373946181
Maprs373946181
PheGenIrs373946181
hapmaprs373946181
1000 genomesrs373946181
hgdprs373946181
ensemblrs373946181
gopubmedrs373946181
geneviewrs373946181
scholarrs373946181
googlers373946181
pharmgkbrs373946181
gwascentralrs373946181
openSNPrs373946181
23andMers373946181
23andMe allrs373946181
SNP Nexus

SNPshotrs373946181
SNPdbers373946181
MSV3drs373946181
GWAS Ctlgrs373946181
Max Magnitude0
ClinVar
Risk rs373946181(A,T;A,T)
Alt rs373946181(A,T;A,T)
Reference rs373946181(C;C)
Significance Pathogenic
Disease Ciliary dyskinesia
Variation info
Gene DNAH11
CLNDBN Ciliary dyskinesia, primary, 7
Reversed 0
HGVS NC_000007.13:g.21745115C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000030678.3,