Variant (rsID / SNP)

rs61734640

rs61734640 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH1. Location: chromosome 3, position 52,390,789. The table records no clinical significance for this variant.

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Reference-table entries

DNAH1Not classified

Variant type: missense_variant
Chromosome / position: 3:52390789
HGVS: NM_015512.5,c.3853C>T,p.Arg1285Trp
Allele change: Missense_R1285W

Associated conditions / phenotypes

Osteoarthritis

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.