Variant (rsID / SNP)

rs4844609

rs4844609 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to CR1. Location: chromosome 1, position 207,782,916. The table records no clinical significance for this variant.

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Reference-table entries

CR1Not classified

Variant type: missense_variant
Chromosome / position: 1:207782916
HGVS: NM_000651.6,c.6178A>T,p.Thr2060Ser
Allele change: Missense_T1610S

Associated conditions / phenotypes

Alzheimer Disease|Mild Cognitive Impairment

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.