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rs786205052

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs786205052(-;-)
Make rs786205052(-;G)
Make rs786205052(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome16
Position84154732
GeneDNAAF1
is asnp
is mentioned by
dbSNPrs786205052
ebirs786205052
HLIrs786205052
Exacrs786205052
Varsomers786205052
Maprs786205052
PheGenIrs786205052
hapmaprs786205052
1000 genomesrs786205052
hgdprs786205052
ensemblrs786205052
gopubmedrs786205052
geneviewrs786205052
scholarrs786205052
googlers786205052
pharmgkbrs786205052
gwascentralrs786205052
openSNPrs786205052
23andMers786205052
23andMe allrs786205052
SNP Nexus

SNPshotrs786205052
SNPdbers786205052
MSV3drs786205052
GWAS Ctlgrs786205052
Max Magnitude0
ClinVar
Risk rs786205052(G;G)
Alt rs786205052(G;G)
Reference rs786205052(;)
Significance Pathogenic
Disease Ciliary dyskinesia
Variation info
Gene DNAAF1
CLNDBN Ciliary dyskinesia, primary, 13
Reversed 0
HGVS NC_000016.9:g.84188337dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000000290.4,