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rs267607225

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607225(C;T)
Make rs267607225(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position84159744
GeneDNAAF1
is asnp
is mentioned by
dbSNPrs267607225
ebirs267607225
HLIrs267607225
Exacrs267607225
Varsomers267607225
Maprs267607225
PheGenIrs267607225
hapmaprs267607225
1000 genomesrs267607225
hgdprs267607225
ensemblrs267607225
gopubmedrs267607225
geneviewrs267607225
scholarrs267607225
googlers267607225
pharmgkbrs267607225
gwascentralrs267607225
openSNPrs267607225
23andMers267607225
23andMe allrs267607225
SNP Nexus

SNPshotrs267607225
SNPdbers267607225
MSV3drs267607225
GWAS Ctlgrs267607225
Max Magnitude0
ClinVar
Risk rs267607225(T;T)
Alt rs267607225(T;T)
Reference rs267607225(C;C)
Significance Pathogenic
Disease Ciliary dyskinesia
Variation info
Gene DNAAF1
CLNDBN Ciliary dyskinesia, primary, 13
Reversed 0
HGVS NC_000016.9:g.84193349C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000000288.3,