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rs727504815

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727504815(G;T)
Make rs727504815(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position49634423
GeneDNAAF2
is asnp
is mentioned by
dbSNPrs727504815
ebirs727504815
HLIrs727504815
Exacrs727504815
Varsomers727504815
Maprs727504815
PheGenIrs727504815
hapmaprs727504815
1000 genomesrs727504815
hgdprs727504815
ensemblrs727504815
gopubmedrs727504815
geneviewrs727504815
scholarrs727504815
googlers727504815
pharmgkbrs727504815
gwascentralrs727504815
openSNPrs727504815
23andMers727504815
23andMe allrs727504815
SNP Nexus

SNPshotrs727504815
SNPdbers727504815
MSV3drs727504815
GWAS Ctlgrs727504815
Max Magnitude0
ClinVar
Risk rs727504815(T;T)
Alt rs727504815(T;T)
Reference rs727504815(G;G)
Significance Probable-Pathogenic
Disease Primary ciliary dyskinesia
Variation info
Gene DNAAF2
CLNDBN Primary ciliary dyskinesia
Reversed 1
HGVS NC_000014.8:g.50101141C>A
CLNSRC
CLNACC RCV000156150.1,