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rs397515622

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515622(G;T)
Make rs397515622(T;T)
ReferenceGRCh38 38.1/141
Chromosome15
Position55491203
GeneDYX1C1, DYX1C1-CCPG1
is asnp
is mentioned by
dbSNPrs397515622
ebirs397515622
HLIrs397515622
Exacrs397515622
Varsomers397515622
Maprs397515622
PheGenIrs397515622
hapmaprs397515622
1000 genomesrs397515622
hgdprs397515622
ensemblrs397515622
gopubmedrs397515622
geneviewrs397515622
scholarrs397515622
googlers397515622
pharmgkbrs397515622
gwascentralrs397515622
openSNPrs397515622
23andMers397515622
23andMe allrs397515622
SNP Nexus

SNPshotrs397515622
SNPdbers397515622
MSV3drs397515622
GWAS Ctlgrs397515622
Max Magnitude0
ClinVar
Risk rs397515622(T;T)
Alt rs397515622(T;T)
Reference rs397515622(G;G)
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.55783401C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000059319.3,