Variant (rsID / SNP)

rs709012

rs709012 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIGLEC1. Location: chromosome 20, position 3,675,498. The table records no clinical significance for this variant.

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Reference-table entries

SIGLEC1Not classified

Variant type: missense_variant
Chromosome / position: 20:3675498
HGVS: NM_023068.4,c.2756A>C,p.His919Pro
Allele change: Missense_H919P

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.