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Variant (rsID / SNP)

rs61742747

HS3ST6

rs61742747 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HS3ST6. Location: chromosome 16, position 1,961,866. The table records no clinical significance for this variant.

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Reference-table entries

HS3ST6Not classified
Variant type
synonymous_variant
Chromosome / position
16:1961866
HGVS
NM_001009606.4,c.754C>T,p.Leu252Leu
Allele change
Synonymous_L252L

Public references

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