Variant (rsID / SNP)

rs190853081

rs190853081 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to APOE. Location: chromosome 19, position 45,412,340. Clinical significance in the table: no interpretation for the single variant.

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Reference-table entries

APOEOther

Clinical significance (as recorded): no interpretation for the single variant
Variant type: single nucleotide variant
Chromosome / position: 19:45412340
Cytoband: 19q13.32
HGVS: NM_000041.4(APOE):c.787G>A (p.Glu263Lys)
Allele change: Missense_E263K

Associated conditions / phenotypes

Cerebral Palsy

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.