Variant (rsID / SNP)

rs2075803

rs2075803 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIGLEC9. Location: chromosome 19, position 51,628,529. The table records no clinical significance for this variant.

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Reference-table entries

SIGLEC9Not classified

Variant type: missense_variant
Chromosome / position: 19:51628529
HGVS: NM_001198558.1,c.298A>G,p.Lys100Glu
Allele change: Missense_K100E

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.