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Variant (rsID / SNP)

rs34767042

D2HGDH

rs34767042 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to D2HGDH. Location: chromosome 2, position 242,688,292. The table records no clinical significance for this variant.

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Reference-table entries

D2HGDHNot classified
Variant type
intron_variant
Chromosome / position
2:242688292
HGVS
NM_152783.5,c.854-1274C>T
Allele change
Silent

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.