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rs797045150

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797045150(A;G)
Make rs797045150(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position55231712
GeneCCNO
is asnp
is mentioned by
dbSNPrs797045150
ebirs797045150
HLIrs797045150
Exacrs797045150
Varsomers797045150
Maprs797045150
PheGenIrs797045150
hapmaprs797045150
1000 genomesrs797045150
hgdprs797045150
ensemblrs797045150
gopubmedrs797045150
geneviewrs797045150
scholarrs797045150
googlers797045150
pharmgkbrs797045150
gwascentralrs797045150
openSNPrs797045150
23andMers797045150
23andMe allrs797045150
SNP Nexus

SNPshotrs797045150
SNPdbers797045150
MSV3drs797045150
GWAS Ctlgrs797045150
Max Magnitude0
ClinVar
Risk rs797045150(G;G)
Alt rs797045150(G;G)
Reference rs797045150(A;A)
Significance Pathogenic
Disease Kartagener syndrome
Variation info
Gene CCNO
CLNDBN Kartagener syndrome
Reversed 1
HGVS NC_000005.9:g.54527540T>C
CLNSRC
CLNACC RCV000190945.1,