Variant (rsID / SNP)
rs41292984
rs41292984 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADGRL2. Location: chromosome 1, position 82,456,585. The table records no clinical significance for this variant.
Reference-table entries
ADGRL2Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:82456585
- HGVS
- NM_001366005.2,c.4166G>A,p.Arg1389Lys
- Allele change
- Missense_R1323K
Associated conditions / phenotypes
Silent|Missense_R1383K
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.