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rs875989825

From SNPedia

Orientationminus
Geno Mag Summary
(TGAA;TGAA) 0 common in clinvar
Make rs875989825(-;-)
Make rs875989825(-;TGAA)
ReferenceGRCh38.p2 38.2/147
Chromosome6
Position158978309
GeneRSPH3
is asnp
is mentioned by
dbSNPrs875989825
ebirs875989825
HLIrs875989825
Exacrs875989825
Varsomers875989825
Maprs875989825
PheGenIrs875989825
hapmaprs875989825
1000 genomesrs875989825
hgdprs875989825
ensemblrs875989825
gopubmedrs875989825
geneviewrs875989825
scholarrs875989825
googlers875989825
pharmgkbrs875989825
gwascentralrs875989825
openSNPrs875989825
23andMers875989825
23andMe allrs875989825
SNP Nexus

SNPshotrs875989825
SNPdbers875989825
MSV3drs875989825
GWAS Ctlgrs875989825
Max Magnitude0
ClinVar
Risk rs875989825(;)
Alt rs875989825(;)
Reference rs875989825(TGAA;TGAA)
Significance Pathogenic
Disease Ciliary dyskinesia
Variation info
Gene RSPH3
CLNDBN Ciliary dyskinesia, primary, 32
Reversed 1
HGVS NC_000006.11:g.159399341_159399344delTTCA
CLNSRC OMIM Allelic Variant
CLNACC RCV000186570.3,