Variant (rsID / SNP)
rs2243372
rs2243372 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FABP7. Location: chromosome 6, position 123,101,647. The table records no clinical significance for this variant.
Reference-table entries
FABP7Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 6:123101647
- HGVS
- NM_001319041.2,c.285A>G,p.Arg95Arg
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.