Variant (rsID / SNP)

rs16987188

rs16987188 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to KIAA1755. Location: chromosome 20, position 36,856,616. The table records no clinical significance for this variant.

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Reference-table entries

KIAA1755Not classified

Variant type: missense_variant
Chromosome / position: 20:36856616
HGVS: NM_001029864.2,c.1898C>T,p.Ala633Val
Allele change: Missense_A633V

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.