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rs606231164

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
(-;AATA) 3 Carrier of a primary ciliary dyskinesia mutation
Make rs606231164(AATA;AATA)
ReferenceGRCh38.p2 38.2/144
Chromosome9
Position34489343
GeneDNAI1
is asnp
is mentioned by
dbSNPrs606231164
dbSNP (classic)rs606231164
ClinGenrs606231164
ebirs606231164
HLIrs606231164
Exacrs606231164
Gnomadrs606231164
Varsomers606231164
LitVarrs606231164
Maprs606231164
PheGenIrs606231164
Biobankrs606231164
1000 genomesrs606231164
hgdprs606231164
ensemblrs606231164
geneviewrs606231164
scholarrs606231164
googlers606231164
pharmgkbrs606231164
gwascentralrs606231164
openSNPrs606231164
23andMers606231164
SNPshotrs606231164
SNPdbers606231164
MSV3drs606231164
GWAS Ctlgrs606231164
Max Magnitude3

aka c.282_283insAATA (p.Gly95Asnfs)

ClinVar
Risk rs606231164(AATA;AATA)
Alt rs606231164(AATA;AATA)
Reference Rs606231164(-;-)
Significance Pathogenic
Disease Kartagener syndrome
Variation info
Gene DNAI1
CLNDBN Kartagener syndrome
Reversed 0
HGVS NC_000009.11:g.34489341_34489342insAATA
CLNSRC OMIM Allelic Variant
CLNACC RCV000005955.4,