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rs797045085

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797045085(C;T)
Make rs797045085(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome7
Position21749750
GeneDNAH11
is asnp
is mentioned by
dbSNPrs797045085
ebirs797045085
HLIrs797045085
Exacrs797045085
Varsomers797045085
Maprs797045085
PheGenIrs797045085
hapmaprs797045085
1000 genomesrs797045085
hgdprs797045085
ensemblrs797045085
gopubmedrs797045085
geneviewrs797045085
scholarrs797045085
googlers797045085
pharmgkbrs797045085
gwascentralrs797045085
openSNPrs797045085
23andMers797045085
23andMe allrs797045085
SNP Nexus

SNPshotrs797045085
SNPdbers797045085
MSV3drs797045085
GWAS Ctlgrs797045085
Max Magnitude0
ClinVar
Risk rs797045085(T;T)
Alt rs797045085(T;T)
Reference rs797045085(C;C)
Significance Pathogenic
Disease Ciliary dyskinesia
Variation info
Gene DNAH11
CLNDBN Ciliary dyskinesia, primary, 7
Reversed 0
HGVS NC_000007.13:g.21789368C>T
CLNSRC
CLNACC RCV000190577.1,