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rs387907151

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs387907151(C;C)
Make rs387907151(C;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position55165904
GeneDNAAF3
is asnp
is mentioned by
dbSNPrs387907151
ebirs387907151
HLIrs387907151
Exacrs387907151
Varsomers387907151
Maprs387907151
PheGenIrs387907151
hapmaprs387907151
1000 genomesrs387907151
hgdprs387907151
ensemblrs387907151
gopubmedrs387907151
geneviewrs387907151
scholarrs387907151
googlers387907151
pharmgkbrs387907151
gwascentralrs387907151
openSNPrs387907151
23andMers387907151
23andMe allrs387907151
SNP Nexus

SNPshotrs387907151
SNPdbers387907151
MSV3drs387907151
GWAS Ctlgrs387907151
Max Magnitude0
ClinVar
Risk rs387907151(C;C)
Alt rs387907151(C;C)
Reference rs387907151(T;T)
Significance Pathogenic
Disease Ciliary dyskinesia Kartagener syndrome
Variation info
Gene DNAAF3
CLNDBN Ciliary dyskinesia, primary, 2 Kartagener syndrome
Reversed 1
HGVS NC_000019.9:g.55677272A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000024243.4, RCV000190868.1,