Variant (rsID / SNP)

rs35677470

rs35677470 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DNASE1L3. Location: chromosome 3, position 58,183,636. The table records no clinical significance for this variant.

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Reference-table entries

DNASE1L3Not classified

Variant type: missense_variant
Chromosome / position: 3:58183636
HGVS: NM_004944.4,c.616C>T,p.Arg206Cys
Allele change: Missense_R176C

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.