Variant (rsID / SNP)
rs17663874
rs17663874 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LDAH. Location: chromosome 2, position 20,885,321. The table records no clinical significance for this variant.
Reference-table entries
LDAHNot classified
- Variant type
- 3_prime_UTR_variant
- Chromosome / position
- 2:20885321
- HGVS
- NM_021925.4,c.*1342G>T
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.