Variant (rsID / SNP)
rs7921977
rs7921977 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CASP7. Location: chromosome 10, position 115,439,569. The table records no clinical significance for this variant.
Reference-table entries
CASP7Not classified
- Variant type
- missense_variant
- Chromosome / position
- 10:115439569
- HGVS
- NM_001267057.1,c.56C>T,p.Thr19Ile
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.