Gene entry
PRDM16
PR/SET domain 16
- Chromosome
- 1
- Cytoband
- 1p36.32
- Variants (rsID)
- 144
PRDM16 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 1 (region 1p36.32). Its official name is “PR/SET domain 16”. The reference table lists 144 variants (rsID) for this gene.
Clinically classified variants
8 reference-table entries with clinical significance.
- rs149333409Benignsingle nucleotide variantLeft ventricular noncompaction 8
- rs187400273Benignsingle nucleotide variantLeft ventricular noncompaction 8
- rs188908415Benignsingle nucleotide variantLeft ventricular noncompaction 8
- rs2244013Benignsingle nucleotide variant
- rs2493292Benignsingle nucleotide variantLeft ventricular noncompaction 8
- rs7535965Benignsingle nucleotide variant
- rs368409902Conflicting interpretationssingle nucleotide variantLeft ventricular noncompaction 8
- rs185041492Likely benignsingle nucleotide variantWolff-Parkinson-White pattern|Left ventricular noncompaction 8
Other listed variants
- rs731031
- rs868688
- rs926244
- rs946760
- rs1890336
- rs2072733
- rs2245703
- rs2455107
- rs2455116
- rs2455135
- rs2455137
- rs2455144
- rs2483239
- rs2483274
- rs2483275
- rs2483278
- rs2483280
- rs2493268
- rs2493272
- rs2493278
- rs2493280
- rs2493284
- rs2493285
- rs2500252
- rs2651895
- rs2651899
- rs2651902
- rs2651909
- rs2651920
- rs2651927
- rs2651935
- rs2742665
- rs2742668
- rs2742687
- rs2788094
- rs2817168
- rs2817178
- rs2817187
- rs2937390
- rs2993482
- rs2993486
- rs2993493
- rs2993501
- rs2993503
- rs3753758
- rs4376672
- rs4415513
- rs4648377
- rs4648379
- rs4648385
- rs4648468
- rs4648487
- rs6658356
- rs6666433
- rs6686156
- rs6687835
- rs6695131
- rs7521730
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.