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rs796052118

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052118(C;T)
Make rs796052118(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position158980867
GeneRSPH3
is asnp
is mentioned by
dbSNPrs796052118
ebirs796052118
HLIrs796052118
Exacrs796052118
Varsomers796052118
Maprs796052118
PheGenIrs796052118
hapmaprs796052118
1000 genomesrs796052118
hgdprs796052118
ensemblrs796052118
gopubmedrs796052118
geneviewrs796052118
scholarrs796052118
googlers796052118
pharmgkbrs796052118
gwascentralrs796052118
openSNPrs796052118
23andMers796052118
23andMe allrs796052118
SNP Nexus

SNPshotrs796052118
SNPdbers796052118
MSV3drs796052118
GWAS Ctlgrs796052118
Max Magnitude0
ClinVar
Risk rs796052118(T;T)
Alt rs796052118(T;T)
Reference rs796052118(C;C)
Significance Pathogenic
Disease Ciliary dyskinesia
Variation info
Gene RSPH3
CLNDBN Ciliary dyskinesia, primary, 32
Reversed 1
HGVS NC_000006.11:g.159401899G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000186569.2,