Variant (rsID / SNP)

rs2278492

rs2278492 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HK3. Location: chromosome 5, position 176,314,459. The table records no clinical significance for this variant.

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Reference-table entries

HK3Not classified

Variant type: synonymous_variant
Chromosome / position: 5:176314459
HGVS: NM_002115.3,c.1593C>T,p.Asp531Asp
Allele change: Synonymous_D531D

Public references

dbSNP
ClinVar
Ensembl
gnomAD

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