Have questions? Visit https://www.reddit.com/r/SNPedia

rs544674332

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs544674332(A;C)
Make rs544674332(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position52353613
GeneDNAH1
is asnp
is mentioned by
dbSNPrs544674332
ebirs544674332
HLIrs544674332
Exacrs544674332
Varsomers544674332
Maprs544674332
PheGenIrs544674332
hapmaprs544674332
1000 genomesrs544674332
hgdprs544674332
ensemblrs544674332
gopubmedrs544674332
geneviewrs544674332
scholarrs544674332
googlers544674332
pharmgkbrs544674332
gwascentralrs544674332
openSNPrs544674332
23andMers544674332
23andMe allrs544674332
SNP Nexus

SNPshotrs544674332
SNPdbers544674332
MSV3drs544674332
GWAS Ctlgrs544674332
Max Magnitude0
ClinVar
Risk rs544674332(C;C)
Alt rs544674332(C;C)
Reference rs544674332(A;A)
Significance Pathogenic
Disease Kartagener syndrome
Variation info
Gene DNAH1
CLNDBN Kartagener syndrome
Reversed 0
HGVS NC_000003.11:g.52387629A>C
CLNSRC
CLNACC RCV000190948.1,