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rs397515621

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515621(C;T)
Make rs397515621(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position55439557
GeneDYX1C1, DYX1C1-CCPG1
is asnp
is mentioned by
dbSNPrs397515621
ebirs397515621
HLIrs397515621
Exacrs397515621
Varsomers397515621
Maprs397515621
PheGenIrs397515621
hapmaprs397515621
1000 genomesrs397515621
hgdprs397515621
ensemblrs397515621
gopubmedrs397515621
geneviewrs397515621
scholarrs397515621
googlers397515621
pharmgkbrs397515621
gwascentralrs397515621
openSNPrs397515621
23andMers397515621
23andMe allrs397515621
SNP Nexus

SNPshotrs397515621
SNPdbers397515621
MSV3drs397515621
GWAS Ctlgrs397515621
Max Magnitude0
ClinVar
Risk rs397515621(T;T)
Alt rs397515621(T;T)
Reference rs397515621(C;C)
Significance Pathogenic
Disease Primary ciliary dyskinesia 25
Variation info
Gene DYX1C1 DYX1C1-CCPG1
CLNDBN Primary ciliary dyskinesia 25
Reversed 1
HGVS NC_000015.9:g.55731755G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000059318.3,