Variant (rsID / SNP)
rs4242746
rs4242746 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PITRM1. Location: chromosome 10, position 3,202,065. The table records no clinical significance for this variant.
Reference-table entries
PITRM1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:3202065
- HGVS
- NM_001242307.2,c.982A>G,p.Ile328Val
- Allele change
- Silent
Associated conditions / phenotypes
Missense_I123V|Missense_I320V|Silent|Silent|Missense_I320V|Missense_I328V|Missense_I296V
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.