Variant (rsID / SNP)
rs75256744
rs75256744 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HOXC4. Location: chromosome 12, position 54,448,106. The table records no clinical significance for this variant.
Reference-table entries
HOXC4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 12:54448106
- HGVS
- NM_014620.6,c.400A>G,p.Ile134Val
- Allele change
- Missense_I134V
Associated conditions / phenotypes
Werner Syndrome|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.