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Variant (rsID / SNP)

rs12924551

DNAH3

rs12924551 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH3. Location: chromosome 16, position 20,966,273. The table records no clinical significance for this variant.

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Reference-table entries

DNAH3Not classified
Variant type
missense_variant
Chromosome / position
16:20966273
HGVS
NM_017539.2,c.10933C>T,p.Arg3645Cys
Allele change
Missense_R3599C

Public references

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