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Variant (rsID / SNP)

rs74000555

PGAP6

rs74000555 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PGAP6. Location: chromosome 16, position 424,288. The table records no clinical significance for this variant.

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Reference-table entries

PGAP6Not classified
Variant type
missense_variant
Chromosome / position
16:424288
HGVS
NM_021259.3,c.1688C>T,p.Ala563Val
Allele change
Missense_A563V

Public references

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