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Variant (rsID / SNP)

rs6037651

SIGLEC1

rs6037651 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIGLEC1. Location: chromosome 20, position 3,686,436. The table records no clinical significance for this variant.

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Reference-table entries

SIGLEC1Not classified
Variant type
missense_variant
Chromosome / position
20:3686436
HGVS
NM_023068.4,c.661G>A,p.Val221Met
Allele change
Missense_V221M

Public references

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