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rs397515461

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515461(C;T)
Make rs397515461(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position132632831
GeneLRRC6
is asnp
is mentioned by
dbSNPrs397515461
ebirs397515461
HLIrs397515461
Exacrs397515461
Varsomers397515461
Maprs397515461
PheGenIrs397515461
hapmaprs397515461
1000 genomesrs397515461
hgdprs397515461
ensemblrs397515461
gopubmedrs397515461
geneviewrs397515461
scholarrs397515461
googlers397515461
pharmgkbrs397515461
gwascentralrs397515461
openSNPrs397515461
23andMers397515461
23andMe allrs397515461
SNP Nexus

SNPshotrs397515461
SNPdbers397515461
MSV3drs397515461
GWAS Ctlgrs397515461
Max Magnitude0
ClinVar
Risk rs397515461(T;T)
Alt rs397515461(T;T)
Reference rs397515461(C;C)
Significance Pathogenic
Disease Ciliary dyskinesia
Variation info
Gene LRRC6
CLNDBN Ciliary dyskinesia, primary, 19
Reversed 1
HGVS NC_000008.10:g.133645077G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000056271.3,