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Variant (rsID / SNP)

rs34924243

SIGLEC1

rs34924243 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIGLEC1. Location: chromosome 20, position 3,682,126. The table records no clinical significance for this variant.

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Reference-table entries

SIGLEC1Not classified
Variant type
missense_variant
Chromosome / position
20:3682126
HGVS
NM_023068.4,c.1391G>A,p.Arg464His
Allele change
Missense_R464H

Public references

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