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rs878854436

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878854436(A;A)
Make rs878854436(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position21868996
GeneDNAH11
is asnp
is mentioned by
dbSNPrs878854436
ebirs878854436
HLIrs878854436
Exacrs878854436
Varsomers878854436
Maprs878854436
PheGenIrs878854436
hapmaprs878854436
1000 genomesrs878854436
hgdprs878854436
ensemblrs878854436
gopubmedrs878854436
geneviewrs878854436
scholarrs878854436
googlers878854436
pharmgkbrs878854436
gwascentralrs878854436
openSNPrs878854436
23andMers878854436
23andMe allrs878854436
SNP Nexus

SNPshotrs878854436
SNPdbers878854436
MSV3drs878854436
GWAS Ctlgrs878854436
Max Magnitude0
ClinVar
Risk rs878854436(A;A)
Alt rs878854436(A;A)
Reference rs878854436(G;G)
Significance Probable-Pathogenic
Disease Primary ciliary dyskinesia
Variation info
Gene DNAH11
CLNDBN Primary ciliary dyskinesia
Reversed 0
HGVS NC_000007.13:g.21908614G>A
CLNSRC
CLNACC RCV000226238.1,