Variant (rsID / SNP)
rs10036727
rs10036727 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLIT3. Location: chromosome 5, position 168,180,081. The table records no clinical significance for this variant.
Reference-table entries
SLIT3Not classified
- Variant type
- missense_variant
- Chromosome / position
- 5:168180081
- HGVS
- NM_001271946.2,c.1852G>A,p.Gly618Ser
- Allele change
- Missense_G618S
Associated conditions / phenotypes
Osteoporosis|Bone Mineral Density Quantitative Trait Locus 15|Bone Mineral Density Quantitative Trait Locus 8
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.