Variant (rsID / SNP)

rs3823430

rs3823430 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH8. Location: chromosome 6, position 38,750,888. The table records no clinical significance for this variant.

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Reference-table entries

DNAH8Not classified

Variant type: missense_variant
Chromosome / position: 6:38750888
HGVS: NM_001206927.2,c.2368A>G,p.Ile790Val
Allele change: Missense_I573V

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.