Variant (rsID / SNP)

rs10899750

rs10899750 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IKZF1. Location: chromosome 7, position 50,436,033. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

IKZF1Not classified

Variant type: missense_variant
Chromosome / position: 7:50436033
HGVS: NM_001291845.2,c.490A>G,p.Arg164Gly
Allele change: Silent

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.