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Variant (rsID / SNP)

rs12364988

SORL1

rs12364988 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SORL1. Location: chromosome 11, position 121,367,626. The table records no clinical significance for this variant.

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Reference-table entries

SORL1Not classified
Variant type
synonymous_variant
Chromosome / position
11:121367626
HGVS
NM_003105.6,c.807T>C,p.His269His
Allele change
Synonymous_H269H

Associated conditions / phenotypes

Alzheimer Disease

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.