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rs397515339

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs397515339(-;-)
Make rs397515339(-;C)
Make rs397515339(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position84170177
GeneDNAAF1
is asnp
is mentioned by
dbSNPrs397515339
ebirs397515339
HLIrs397515339
Exacrs397515339
Varsomers397515339
Maprs397515339
PheGenIrs397515339
hapmaprs397515339
1000 genomesrs397515339
hgdprs397515339
ensemblrs397515339
gopubmedrs397515339
geneviewrs397515339
scholarrs397515339
googlers397515339
pharmgkbrs397515339
gwascentralrs397515339
openSNPrs397515339
23andMers397515339
23andMe allrs397515339
SNP Nexus

SNPshotrs397515339
SNPdbers397515339
MSV3drs397515339
GWAS Ctlgrs397515339
Max Magnitude0
ClinVar
Risk rs397515339(C;C)
Alt rs397515339(C;C)
Reference rs397515339(;)
Significance Pathogenic
Disease Ciliary dyskinesia Kartagener syndrome
Variation info
Gene DNAAF1
CLNDBN Ciliary dyskinesia, primary, 13 Kartagener syndrome
Reversed 0
HGVS NC_000016.9:g.84203783dupC
CLNSRC OMIM Allelic Variant
CLNACC RCV000000287.5, RCV000190867.1,