Variant (rsID / SNP)

rs28362581

rs28362581 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AMPD2. Location: chromosome 1, position 110,163,879. The table records no clinical significance for this variant.

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Reference-table entries

AMPD2Not classified

Variant type: missense_variant
Chromosome / position: 1:110163879
HGVS: NM_001368809.2,c.82G>A,p.Ala28Thr
Allele change: Missense_A82T

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.