Variant (rsID / SNP)

rs10828663

rs10828663 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIAA1217. Location: chromosome 10, position 24,813,454. The table records no clinical significance for this variant.

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Reference-table entries

KIAA1217Not classified

Variant type: missense_variant
Chromosome / position: 10:24813454
HGVS: NM_019590.5,c.2659G>A,p.Ala887Thr
Allele change: Missense_A807T

Associated conditions / phenotypes

Missense_A570T|Missense_A570T

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.