Variant (rsID / SNP)
rs10416265
rs10416265 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPATCH1. Location: chromosome 19, position 33,605,300. The table records no clinical significance for this variant.
Reference-table entries
GPATCH1Not classified
- Variant type
- missense_variant
- Chromosome / position
- 19:33605300
- HGVS
- NM_018025.3,c.2171A>G,p.His724Arg
- Allele change
- Missense_H724R
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.