Variant (rsID / SNP)

rs61749651

rs61749651 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HK3. Location: chromosome 5, position 176,314,206. The table records no clinical significance for this variant.

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Reference-table entries

HK3Not classified

Variant type: missense_variant
Chromosome / position: 5:176314206
HGVS: NM_002115.3,c.1733A>G,p.Gln578Arg
Allele change: Missense_Q578R

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.