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rs397515413

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515413(G;T)
Make rs397515413(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position70988133
GeneHYDIN
is asnp
is mentioned by
dbSNPrs397515413
ebirs397515413
HLIrs397515413
Exacrs397515413
Varsomers397515413
Maprs397515413
PheGenIrs397515413
hapmaprs397515413
1000 genomesrs397515413
hgdprs397515413
ensemblrs397515413
gopubmedrs397515413
geneviewrs397515413
scholarrs397515413
googlers397515413
pharmgkbrs397515413
gwascentralrs397515413
openSNPrs397515413
23andMers397515413
23andMe allrs397515413
SNP Nexus

SNPshotrs397515413
SNPdbers397515413
MSV3drs397515413
GWAS Ctlgrs397515413
Max Magnitude0
ClinVar
Risk rs397515413(T;T)
Alt rs397515413(T;T)
Reference rs397515413(G;G)
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.71022036C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000032900.6, RCV000190872.1,