Variant (rsID / SNP)

rs141831656

rs141831656 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to HS3ST3A1. Location: chromosome 17, position 13,399,884. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

HS3ST3A1Not classified

Variant type: missense_variant
Chromosome / position: 17:13399884
HGVS: NM_006042.3,c.851G>A,p.Ser284Asn
Allele change: Missense_S284N

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.