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rs373501414

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs373501414(A;A)
Make rs373501414(A;C)
ReferenceGRCh38 38.1/142
Chromosome16
Position70991397
GeneHYDIN
is asnp
is mentioned by
dbSNPrs373501414
ebirs373501414
HLIrs373501414
Exacrs373501414
Varsomers373501414
Maprs373501414
PheGenIrs373501414
hapmaprs373501414
1000 genomesrs373501414
hgdprs373501414
ensemblrs373501414
gopubmedrs373501414
geneviewrs373501414
scholarrs373501414
googlers373501414
pharmgkbrs373501414
gwascentralrs373501414
openSNPrs373501414
23andMers373501414
23andMe allrs373501414
SNP Nexus

SNPshotrs373501414
SNPdbers373501414
MSV3drs373501414
GWAS Ctlgrs373501414
Max Magnitude0
ClinVar
Risk rs373501414(A;A)
Alt rs373501414(A;A)
Reference rs373501414(C;C)
Significance Pathogenic
Disease Ciliary dyskinesia
Variation info
Gene HYDIN
CLNDBN Ciliary dyskinesia, primary, 5
Reversed 0
HGVS NC_000016.9:g.71025300C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000055663.3,