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rs141581673

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs141581673(A;A)
Make rs141581673(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position74312024
GeneDNAI2, LOC105371891
is asnp
is mentioned by
dbSNPrs141581673
dbSNP (old)rs141581673
ClinGenrs141581673
ebirs141581673
HLIrs141581673
Exacrs141581673
Gnomadrs141581673
Varsomers141581673
LitVarrs141581673
Maprs141581673
PheGenIrs141581673
Biobankrs141581673
1000 genomesrs141581673
hgdprs141581673
ensemblrs141581673
gopubmedrs141581673
geneviewrs141581673
scholarrs141581673
googlers141581673
pharmgkbrs141581673
gwascentralrs141581673
openSNPrs141581673
23andMers141581673
23andMe allrs141581673
SNPshotrs141581673
SNPdbers141581673
MSV3drs141581673
GWAS Ctlgrs141581673
Max Magnitude0
ClinVar
Risk rs141581673(A;A) rs141581673(T;T)
Alt rs141581673(A;A) rs141581673(T;T)
Reference Rs141581673(C;C)
Significance Pathogenic
Disease Primary ciliary dyskinesia
Variation info
Gene DNAI2
CLNDBN Primary ciliary dyskinesia
Reversed 0
HGVS NC_000017.10:g.72308163C>T
CLNSRC
CLNACC RCV000456361.1,