Variant (rsID / SNP)
rs6901
rs6901 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PITRM1. Location: chromosome 10, position 3,180,227. The table records no clinical significance for this variant.
Reference-table entries
PITRM1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:3180227
- HGVS
- NM_001242307.2,c.3113A>G,p.Gln1038Arg
- Allele change
- Silent
Associated conditions / phenotypes
Missense_Q766R|Missense_Q1029R|Silent|Silent|Missense_Q963R|Missense_Q1037R|Missense_Q939R
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.