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Variant (rsID / SNP)

rs77634238

DNAH3

rs77634238 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNAH3. Location: chromosome 16, position 21,123,315. The table records no clinical significance for this variant.

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Reference-table entries

DNAH3Not classified
Variant type
missense_variant&splice_region_variant
Chromosome / position
16:21123315
HGVS
NM_017539.2,c.1919C>T,p.Thr640Met
Allele change
Missense_T580M

Public references

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