Variant (rsID / SNP)

rs10769699

rs10769699 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNHD1, RRP8. Location: chromosome 11, position 6,588,228. The table records no clinical significance for this variant.

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Reference-table entries

DNHD1Not classified

Variant type: missense_variant
Chromosome / position: 11:6588228
HGVS: NM_144666.3,c.11489G>A,p.Arg3830His
Allele change: Missense_R3830H

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.