Variant (rsID / SNP)

rs9516771

rs9516771 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HS6ST3. Location: chromosome 13, position 97,484,830. The table records no clinical significance for this variant.

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Reference-table entries

HS6ST3Not classified

Variant type: missense_variant
Chromosome / position: 13:97484830
HGVS: NM_153456.4,c.794A>G,p.Lys265Arg
Allele change: Missense_K265R

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.