Variant (rsID / SNP)
rs2275363
rs2275363 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to RAP1GAP. Location: chromosome 1, position 21,940,555. The table records no clinical significance for this variant.
Reference-table entries
RAP1GAPNot classified
- Variant type
- missense_variant
- Chromosome / position
- 1:21940555
- HGVS
- NM_001388200.1,c.319G>A,p.Ala107Thr
- Allele change
- Missense_A107T
Associated conditions / phenotypes
Missense_A107T|Missense_A107T|Missense_A107T|Missense_A107T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.