Gene entry
P3H2
prolyl 3-hydroxylase 2
- Chromosome
- 3
- Cytoband
- 3q28
- Variants (rsID)
- 48
P3H2 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 3 (region 3q28). Its official name is “prolyl 3-hydroxylase 2”. The reference table lists 48 variants (rsID) for this gene.
Clinically classified variants
1 reference-table entries with clinical significance.
- rs117688924Conflicting interpretationssingle nucleotide variantMyopia, high, with cataract and vitreoretinal degeneration
Other listed variants
- rs710574
- rs710576
- rs710586
- rs710589
- rs710590
- rs710595
- rs837674
- rs837682
- rs837766
- rs863923
- rs1018343
- rs1349036
- rs1403416
- rs1962321
- rs1985690
- rs2378562
- rs3108306
- rs3773932
- rs3773936
- rs6767660
- rs6773019
- rs7610141
- rs7639633
- rs9876409
- rs13096237
- rs16865070
- rs35072845
- rs56026146
- rs62279648
- rs73184354
- rs73186433
- rs74992786
- rs75374438
- rs75523528
- rs77265128
- rs79592707
- rs79634405
- rs112980716
- rs114582878
- rs115596050
- rs115857659
- rs116315439
- rs116826435
- rs117111077
- rs141401355
- rs183732333
- rs199877373
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.