Variant (rsID / SNP)

rs72780891

rs72780891 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH3. Location: chromosome 16, position 21,151,913. The table records no clinical significance for this variant.

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Reference-table entries

DNAH3Not classified

Variant type: missense_variant
Chromosome / position: 16:21151913
HGVS: NM_017539.2,c.640C>A,p.Gln214Lys
Allele change: Missense_Q185K

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.