Variant (rsID / SNP)
rs1054627
rs1054627 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IBSP. Location: chromosome 4, position 88,732,692. The table records no clinical significance for this variant.
Reference-table entries
IBSPNot classified
- Variant type
- missense_variant
- Chromosome / position
- 4:88732692
- HGVS
- NM_004967.4,c.584G>A,p.Gly195Glu
- Allele change
- Missense_G195E
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.