Variant (rsID / SNP)

rs12929546

rs12929546 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH3. Location: chromosome 16, position 20,981,162. The table records no clinical significance for this variant.

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Reference-table entries

DNAH3Not classified

Variant type: missense_variant
Chromosome / position: 16:20981162
HGVS: NM_017539.2,c.8410A>G,p.Ile2804Val
Allele change: Missense_I2758V

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.