Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Variant (rsID / SNP)

rs611847

SIGLEC1

rs611847 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIGLEC1. Location: chromosome 20, position 3,684,022. The table records no clinical significance for this variant.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Reference-table entries

SIGLEC1Not classified
Variant type
synonymous_variant
Chromosome / position
20:3684022
HGVS
NM_023068.4,c.1050T>C,p.Asn350Asn
Allele change
Synonymous_N350N

Public references

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