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rs1060503063

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1060503063(C;T)
Make rs1060503063(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome7
Position21842641
GeneDNAH11
is asnp
is mentioned by
dbSNPrs1060503063
dbSNP (classic)rs1060503063
ClinGenrs1060503063
ebirs1060503063
HLIrs1060503063
Exacrs1060503063
Gnomadrs1060503063
Varsomers1060503063
LitVarrs1060503063
Maprs1060503063
PheGenIrs1060503063
Biobankrs1060503063
1000 genomesrs1060503063
hgdprs1060503063
ensemblrs1060503063
geneviewrs1060503063
scholarrs1060503063
googlers1060503063
pharmgkbrs1060503063
gwascentralrs1060503063
openSNPrs1060503063
23andMers1060503063
23andMe allrs1060503063
SNPshotrs1060503063
SNPdbers1060503063
MSV3drs1060503063
GWAS Ctlgrs1060503063
Max Magnitude0
ClinVar
Risk rs1060503063(T;T)
Alt rs1060503063(T;T)
Reference Rs1060503063(C;C)
Significance Pathogenic
Disease Primary ciliary dyskinesia
Variation info
Gene DNAH11
CLNDBN Primary ciliary dyskinesia
Reversed 0
HGVS NC_000007.13:g.21882259C>T
CLNSRC
CLNACC RCV000459493.1,