Variant (rsID / SNP)
rs34494334
rs34494334 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to R3HCC1L. Location: chromosome 10, position 99,969,475. The table records no clinical significance for this variant.
Reference-table entries
R3HCC1LNot classified
- Variant type
- missense_variant
- Chromosome / position
- 10:99969475
- HGVS
- NM_001256619.2,c.1604A>C,p.Asp535Ala
- Allele change
- Missense_D535A
Associated conditions / phenotypes
Missense_D535A|Missense_D535A|Missense_D535A|Missense_D535A|Missense_D535A|Missense_D535A|Missense_D535A|Missense_D535A
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.