Variant (rsID / SNP)
rs1531111
rs1531111 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HECW2. Location: chromosome 2, position 197,184,321. The table records no clinical significance for this variant.
Reference-table entries
HECW2Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 2:197184321
- HGVS
- NM_001348768.2,c.1293G>A,p.Pro431Pro
- Allele change
- Synonymous_P431P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.