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rs142371860

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs142371860(C;T)
Make rs142371860(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position26421396
GeneDRC1
is asnp
is mentioned by
dbSNPrs142371860
ebirs142371860
HLIrs142371860
Exacrs142371860
Varsomers142371860
Maprs142371860
PheGenIrs142371860
hapmaprs142371860
1000 genomesrs142371860
hgdprs142371860
ensemblrs142371860
gopubmedrs142371860
geneviewrs142371860
scholarrs142371860
googlers142371860
pharmgkbrs142371860
gwascentralrs142371860
openSNPrs142371860
23andMers142371860
23andMe allrs142371860
SNP Nexus

SNPshotrs142371860
SNPdbers142371860
MSV3drs142371860
GWAS Ctlgrs142371860
Max Magnitude0
ClinVar
Risk rs142371860(A,T;A,T)
Alt rs142371860(A,T;A,T)
Reference rs142371860(C;C)
Significance Pathogenic
Disease Ciliary dyskinesia Kartagener syndrome
Variation info
Gene DRC1
CLNDBN Ciliary dyskinesia, primary, 21 Kartagener syndrome
Reversed 0
HGVS NC_000002.11:g.26644264C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000049261.3, RCV000190935.1,