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rs773801386

From SNPedia

Orientationplus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Make rs773801386(-;-)
Make rs773801386(-;TG)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position180654861
GeneCCDC39
is asnp
is mentioned by
dbSNPrs773801386
ebirs773801386
HLIrs773801386
Exacrs773801386
Varsomers773801386
Maprs773801386
PheGenIrs773801386
hapmaprs773801386
1000 genomesrs773801386
hgdprs773801386
ensemblrs773801386
gopubmedrs773801386
geneviewrs773801386
scholarrs773801386
googlers773801386
pharmgkbrs773801386
gwascentralrs773801386
openSNPrs773801386
23andMers773801386
23andMe allrs773801386
SNP Nexus

SNPshotrs773801386
SNPdbers773801386
MSV3drs773801386
GWAS Ctlgrs773801386
Max Magnitude0
ClinVar
Risk rs773801386(;)
Alt rs773801386(;)
Reference rs773801386(TG;TG)
Significance Pathogenic
Disease Primary ciliary dyskinesia
Variation info
Gene CCDC39
CLNDBN Primary ciliary dyskinesia
Reversed 0
HGVS NC_000003.11:g.180372649_180372650delTG
CLNSRC
CLNACC RCV000226980.1,