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rs587776997

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs587776997(A;T)
Make rs587776997(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position26454783
GeneDRC1
is asnp
is mentioned by
dbSNPrs587776997
ebirs587776997
HLIrs587776997
Exacrs587776997
Varsomers587776997
Maprs587776997
PheGenIrs587776997
hapmaprs587776997
1000 genomesrs587776997
hgdprs587776997
ensemblrs587776997
gopubmedrs587776997
geneviewrs587776997
scholarrs587776997
googlers587776997
pharmgkbrs587776997
gwascentralrs587776997
openSNPrs587776997
23andMers587776997
23andMe allrs587776997
SNP Nexus

SNPshotrs587776997
SNPdbers587776997
MSV3drs587776997
GWAS Ctlgrs587776997
Max Magnitude0
ClinVar
Risk rs587776997(T;T)
Alt rs587776997(T;T)
Reference rs587776997(A;A)
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.26677651A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000049260.3, RCV000190936.1,