Variant (rsID / SNP)
rs80345791
rs80345791 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARHGAP22. Location: chromosome 10, position 49,659,006. The table records no clinical significance for this variant.
Reference-table entries
ARHGAP22Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:49659006
- HGVS
- NM_001256024.2,c.1214C>T,p.Pro405Leu
- Allele change
- Missense_P395L
Associated conditions / phenotypes
Missense_P395L|Missense_P346L|Silent|Missense_P389L|Missense_P299L
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.