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rs878854446

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878854446(C;G)
Make rs878854446(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position21748679
GeneDNAH11
is asnp
is mentioned by
dbSNPrs878854446
ebirs878854446
HLIrs878854446
Exacrs878854446
Varsomers878854446
Maprs878854446
PheGenIrs878854446
hapmaprs878854446
1000 genomesrs878854446
hgdprs878854446
ensemblrs878854446
gopubmedrs878854446
geneviewrs878854446
scholarrs878854446
googlers878854446
pharmgkbrs878854446
gwascentralrs878854446
openSNPrs878854446
23andMers878854446
23andMe allrs878854446
SNP Nexus

SNPshotrs878854446
SNPdbers878854446
MSV3drs878854446
GWAS Ctlgrs878854446
Max Magnitude0
ClinVar
Risk rs878854446(G;G)
Alt rs878854446(G;G)
Reference rs878854446(C;C)
Significance Pathogenic
Disease Primary ciliary dyskinesia
Variation info
Gene DNAH11
CLNDBN Primary ciliary dyskinesia
Reversed 0
HGVS NC_000007.13:g.21788297C>G
CLNSRC
CLNACC RCV000233638.1,