Variant (rsID / SNP)
rs3813722
rs3813722 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AFAP1L2. Location: chromosome 10, position 116,073,696. The table records no clinical significance for this variant.
Reference-table entries
AFAP1L2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 10:116073696
- HGVS
- NM_001287824.2,c.885G>A,p.Thr295Thr
- Allele change
- Synonymous_T270T
Associated conditions / phenotypes
Synonymous_T270T|Synonymous_T242T|Synonymous_T242T|Synonymous_T270T|Synonymous_T270T|Synonymous_T242T|Synonymous_T214T|Synonymous_T260T|Synonymous_T186T|Synonymous_T295T|Synonymous_T242T|Synonymous_T242T|Synonymous_T214T|Synonymous_T242T|Synonymous_T270T
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.