Variant (rsID / SNP)

rs3829658

rs3829658 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIGLEC12. Location: chromosome 19, position 52,000,672. The table records no clinical significance for this variant.

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Reference-table entries

SIGLEC12Not classified

Variant type: missense_variant
Chromosome / position: 19:52000672
HGVS: NM_053003.4,c.1433C>T,p.Thr478Met
Allele change: Missense_T360M

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.