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rs797045147

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs797045147(-;C)
Make rs797045147(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position116616789
GeneRSPH4A
is asnp
is mentioned by
dbSNPrs797045147
ClinGenrs797045147
ebirs797045147
HLIrs797045147
Exacrs797045147
Varsomers797045147
Maprs797045147
PheGenIrs797045147
hapmaprs797045147
1000 genomesrs797045147
hgdprs797045147
ensemblrs797045147
gopubmedrs797045147
geneviewrs797045147
scholarrs797045147
googlers797045147
pharmgkbrs797045147
gwascentralrs797045147
openSNPrs797045147
23andMers797045147
23andMe allrs797045147
SNP Nexus

SNPshotrs797045147
SNPdbers797045147
MSV3drs797045147
GWAS Ctlgrs797045147
Max Magnitude0
ClinVar
Risk rs797045147(C;C)
Alt rs797045147(C;C)
Reference Rs797045147(-;-)
Significance Pathogenic
Disease Kartagener syndrome
Variation info
Gene RSPH4A
CLNDBN Kartagener syndrome
Reversed 0
HGVS NC_000006.11:g.116937952dupC
CLNSRC
CLNACC RCV000190912.1,