Variant (rsID / SNP)
rs2275875
rs2275875 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DHRS3. Location: chromosome 1, position 12,638,964. The table records no clinical significance for this variant.
Reference-table entries
DHRS3Not classified
- Variant type
- synonymous_variant
- Chromosome / position
- 1:12638964
- HGVS
- NM_004753.7,c.480A>G,p.Pro160Pro
- Allele change
- Synonymous_P160P
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.
