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rs797045146

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
(I;I) 0 common genotype
Make rs797045146(-;-)
Make rs797045146(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position49635119
GeneDNAAF2
is asnp
is mentioned by
dbSNPrs797045146
dbSNP (classic)rs797045146
ClinGenrs797045146
ebirs797045146
HLIrs797045146
Exacrs797045146
Gnomadrs797045146
Varsomers797045146
LitVarrs797045146
Maprs797045146
PheGenIrs797045146
Biobankrs797045146
1000 genomesrs797045146
hgdprs797045146
ensemblrs797045146
geneviewrs797045146
scholarrs797045146
googlers797045146
pharmgkbrs797045146
gwascentralrs797045146
openSNPrs797045146
23andMers797045146
SNPshotrs797045146
SNPdbers797045146
MSV3drs797045146
GWAS Ctlgrs797045146
Max Magnitude0
ClinVar
Risk rs797045146(-;-)
Alt rs797045146(-;-)
Reference Rs797045146(G;G)
Significance Pathogenic
Disease Kartagener syndrome
Variation info
Gene DNAAF2
CLNDBN Kartagener syndrome
Reversed 1
HGVS NC_000014.8:g.50101837delC
CLNSRC
CLNACC RCV000190911.1,