Variant (rsID / SNP)
rs1671021
rs1671021 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LLGL2. Location: chromosome 17, position 73,565,171. The table records no clinical significance for this variant.
Reference-table entries
LLGL2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 17:73565171
- HGVS
- NM_001031803.2,c.1435T>C,p.Phe479Leu
- Allele change
- Missense_F479L
Associated conditions / phenotypes
Hypertension, Essential|Body Mass Index Quantitative Trait Locus 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.