Variant (rsID / SNP)
rs10901772
rs10901772 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LHPP. Location: chromosome 10, position 126,268,371. The table records no clinical significance for this variant.
Reference-table entries
LHPPNot classified
- Variant type
- intron_variant
- Chromosome / position
- 10:126268371
- HGVS
- NM_022126.4,c.717-33462T>C
- Allele change
- Silent
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.