Gene entry
XDH
xanthine dehydrogenase
- Chromosome
- 2
- Cytoband
- 2p23.1
- Variants (rsID)
- 79
XDH is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 2 (region 2p23.1). Its official name is “xanthine dehydrogenase”. The reference table lists 79 variants (rsID) for this gene.
Clinically classified variants
18 reference-table entries with clinical significance.
- rs1366813Benignsingle nucleotide variantHereditary xanthinuria type 1|Xanthinuria type II
- rs17011368Benignsingle nucleotide variantHereditary xanthinuria type 1|Xanthinuria type II
- rs17323225Benignsingle nucleotide variantHereditary xanthinuria type 1|Xanthinuria type II
- rs1884725Benignsingle nucleotide variantHereditary xanthinuria type 1|Xanthinuria type II
- rs207440Benignsingle nucleotide variantHereditary xanthinuria type 1|Xanthinuria type II
- rs2295475Benignsingle nucleotide variantHereditary xanthinuria type 1|Xanthinuria type II
- rs34929837Benignsingle nucleotide variantHereditary xanthinuria type 1|Xanthinuria type II
- rs4407290Benignsingle nucleotide variantHereditary xanthinuria type 1|Xanthinuria type II
- rs45488100Benignsingle nucleotide variantHereditary xanthinuria type 1
- rs45523133Benignsingle nucleotide variantHereditary xanthinuria type 1|Xanthinuria type II
- rs45575032Benignsingle nucleotide variantHereditary xanthinuria type 1|Xanthinuria type II
- rs6710015Benignsingle nucleotide variantHereditary xanthinuria type 1
- rs138649664Conflicting interpretationssingle nucleotide variantHereditary xanthinuria type 1|Xanthinuria type II
- rs148412639Conflicting interpretationssingle nucleotide variantHereditary xanthinuria type 1|Xanthinuria type II
- rs45442092Likely benignsingle nucleotide variantXanthinuria type II|Hereditary xanthinuria type 1
- rs72549369Pathogenicsingle nucleotide variantHereditary xanthinuria type 1
- rs145064943Uncertain significancesingle nucleotide variantXanthinuria type II
- rs145413551Uncertain significancesingle nucleotide variantXanthinuria type II
Other listed variants
- rs207454
- rs207455
- rs494852
- rs561525
- rs732436
- rs992137
- rs992138
- rs1429376
- rs1594160
- rs1864280
- rs2043013
- rs2236168
- rs2268801
- rs2295474
- rs4951978
- rs9308919
- rs17011401
- rs45471100
- rs45471294
- rs45503198
- rs45504106
- rs45528140
- rs45547640
- rs45549632
- rs45557040
- rs45564939
- rs45577338
- rs45579134
- rs45596633
- rs45624433
- rs45626033
- rs55676250
- rs56385520
- rs72790632
- rs72790636
- rs114001426
- rs114259258
- rs116290580
- rs138633733
- rs139515054
- rs139750654
- rs141667019
- rs142217309
- rs143124863
- rs143887178
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.