Variant (rsID / SNP)
rs3814596
rs3814596 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PITRM1. Location: chromosome 10, position 3,207,632. The table records no clinical significance for this variant.
Reference-table entries
PITRM1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:3207632
- HGVS
- NM_001242307.2,c.506T>C,p.Phe169Ser
- Allele change
- Silent
Associated conditions / phenotypes
Missense_F161S|Silent|Silent|Missense_F161S|Missense_F169S|Missense_F137S
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.