Variant (rsID / SNP)
rs351111
rs351111 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PRTN3. Location: chromosome 19, position 844,020. The table records no clinical significance for this variant.
Reference-table entries
PRTN3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:844020
- HGVS
- NM_002777.4,c.355G>A,p.Val119Ile
- Allele change
- Missense_V119I
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.