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Variant (rsID / SNP)

rs12449649

ABCA5

rs12449649 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA5. Location: chromosome 17, position 67,260,926. The table records no clinical significance for this variant.

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Reference-table entries

ABCA5Not classified
Variant type
synonymous_variant
Chromosome / position
17:67260926
HGVS
NM_018672.5,c.3265T>C,p.Leu1089Leu
Allele change
Synonymous_L1089L

Public references

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