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rs567050969

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs567050969(C;T)
Make rs567050969(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome6
Position38786788
GeneDNAH8
is asnp
is mentioned by
dbSNPrs567050969
ebirs567050969
HLIrs567050969
Exacrs567050969
Varsomers567050969
Maprs567050969
PheGenIrs567050969
hapmaprs567050969
1000 genomesrs567050969
hgdprs567050969
ensemblrs567050969
gopubmedrs567050969
geneviewrs567050969
scholarrs567050969
googlers567050969
pharmgkbrs567050969
gwascentralrs567050969
openSNPrs567050969
23andMers567050969
23andMe allrs567050969
SNP Nexus

SNPshotrs567050969
SNPdbers567050969
MSV3drs567050969
GWAS Ctlgrs567050969
Max Magnitude0
ClinVar
Risk rs567050969(T;T)
Alt rs567050969(T;T)
Reference rs567050969(C;C)
Significance Pathogenic
Disease not provided Kartagener syndrome
Variation info
Gene DNAH8
CLNDBN not provided Kartagener syndrome
Reversed 0
HGVS NC_000006.11:g.38754564C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000144929.3, RCV000190949.1,