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rs397515414

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397515414(A;T)
Make rs397515414(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position71137272
GeneHYDIN
is asnp
is mentioned by
dbSNPrs397515414
ebirs397515414
HLIrs397515414
Exacrs397515414
Varsomers397515414
Maprs397515414
PheGenIrs397515414
hapmaprs397515414
1000 genomesrs397515414
hgdprs397515414
ensemblrs397515414
gopubmedrs397515414
geneviewrs397515414
scholarrs397515414
googlers397515414
pharmgkbrs397515414
gwascentralrs397515414
openSNPrs397515414
23andMers397515414
23andMe allrs397515414
SNP Nexus

SNPshotrs397515414
SNPdbers397515414
MSV3drs397515414
GWAS Ctlgrs397515414
Max Magnitude0
ClinVar
Risk rs397515414(T;T)
Alt rs397515414(T;T)
Reference rs397515414(A;A)
Significance Pathogenic
Disease Ciliary dyskinesia Kartagener syndrome
Variation info
Gene HYDIN
CLNDBN Ciliary dyskinesia, primary, 5 Kartagener syndrome
Reversed 1
HGVS NC_000016.9:g.71171175T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000032901.4, RCV000190871.1,