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rs121908855

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121908855(C;G)
Make rs121908855(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position21880869
GeneDNAH11
is asnp
is mentioned by
dbSNPrs121908855
ebirs121908855
HLIrs121908855
Exacrs121908855
Varsomers121908855
Maprs121908855
PheGenIrs121908855
hapmaprs121908855
1000 genomesrs121908855
hgdprs121908855
ensemblrs121908855
gopubmedrs121908855
geneviewrs121908855
scholarrs121908855
googlers121908855
pharmgkbrs121908855
gwascentralrs121908855
openSNPrs121908855
23andMers121908855
23andMe allrs121908855
SNP Nexus

SNPshotrs121908855
SNPdbers121908855
MSV3drs121908855
GWAS Ctlgrs121908855
Max Magnitude0
OMIM603339
Desc
Variant0002
Relatedalso
ClinVar
Risk rs121908855(G;G)
Alt rs121908855(G;G)
Reference rs121908855(C;C)
Significance Pathogenic
Disease Ciliary dyskinesia
Variation info
Gene DNAH11
CLNDBN Ciliary dyskinesia, primary, 7
Reversed 0
HGVS NC_000007.13:g.21920487C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000006848.4,