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rs587777780

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587777780(G;T)
Make rs587777780(T;T)
ReferenceGRCh38 38.1/142
Chromosome19
Position11422722
GeneCCDC151
is asnp
is mentioned by
dbSNPrs587777780
ebirs587777780
HLIrs587777780
Exacrs587777780
Varsomers587777780
Maprs587777780
PheGenIrs587777780
hapmaprs587777780
1000 genomesrs587777780
hgdprs587777780
ensemblrs587777780
gopubmedrs587777780
geneviewrs587777780
scholarrs587777780
googlers587777780
pharmgkbrs587777780
gwascentralrs587777780
openSNPrs587777780
23andMers587777780
23andMe allrs587777780
SNP Nexus

SNPshotrs587777780
SNPdbers587777780
MSV3drs587777780
GWAS Ctlgrs587777780
Max Magnitude0
ClinVar
Risk rs587777780(T;T)
Alt rs587777780(T;T)
Reference rs587777780(G;G)
Significance Pathogenic
Disease Ciliary dyskinesia Kartagener syndrome
Variation info
Gene CCDC151
CLNDBN Ciliary dyskinesia, primary, 30 Kartagener syndrome
Reversed 0
HGVS NC_000019.9:g.11533390G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000144450.3, RCV000190933.1,