Variant (rsID / SNP)

rs10490924

rs10490924 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ARMS2. Location: chromosome 10, position 124,214,448. Clinical significance in the table: Benign.

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Reference-table entries

ARMS2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:124214448
Cytoband: 10q26.13
HGVS: NM_001099667.3(ARMS2):c.205G>T (p.Ala69Ser)
Allele change: Missense_A69S

Associated conditions / phenotypes

Age related macular degeneration 8

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.