Variant (rsID / SNP)

rs11668530

rs11668530 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SIGLEC12. Location: chromosome 19, position 52,001,485. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SIGLEC12Not classified

Variant type: missense_variant
Chromosome / position: 19:52001485
HGVS: NM_053003.4,c.1192C>T,p.His398Tyr
Allele change: Missense_H280Y

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.