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Variant (rsID / SNP)

rs12535

DAPL1

rs12535 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DAPL1. Location: chromosome 2, position 159,663,616. The table records no clinical significance for this variant.

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Reference-table entries

DAPL1Not classified
Variant type
missense_variant
Chromosome / position
2:159663616
HGVS
NM_001017920.3,c.196G>A,p.Ala66Thr
Allele change
Missense_A66T

Public references

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