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Variant (rsID / SNP)

rs489172

ZP1

rs489172 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ZP1. Location: chromosome 11, position 60,637,164. The table records no clinical significance for this variant.

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Reference-table entries

ZP1Not classified
Variant type
missense_variant
Chromosome / position
11:60637164
HGVS
NM_207341.4,c.473C>T,p.Thr158Ile
Allele change
Missense_T158I

Public references

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