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rs863224519

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224519(A;T)
Make rs863224519(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome17
Position80097320
GeneCCDC40, MIR1268B
is asnp
is mentioned by
dbSNPrs863224519
ebirs863224519
HLIrs863224519
Exacrs863224519
Varsomers863224519
Maprs863224519
PheGenIrs863224519
hapmaprs863224519
1000 genomesrs863224519
hgdprs863224519
ensemblrs863224519
gopubmedrs863224519
geneviewrs863224519
scholarrs863224519
googlers863224519
pharmgkbrs863224519
gwascentralrs863224519
openSNPrs863224519
23andMers863224519
23andMe allrs863224519
SNP Nexus

SNPshotrs863224519
SNPdbers863224519
MSV3drs863224519
GWAS Ctlgrs863224519
Max Magnitude0
ClinVar
Risk rs863224519(T;T)
Alt rs863224519(T;T)
Reference rs863224519(A;A)
Significance Pathogenic
Disease Primary ciliary dyskinesia
Variation info
Gene MIR1268B CCDC40
CLNDBN Primary ciliary dyskinesia
Reversed 0
HGVS NC_000017.10:g.78071119A>T
CLNSRC
CLNACC RCV000196101.2,