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Variant (rsID / SNP)

rs2228331

GPC1

rs2228331 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPC1. Location: chromosome 2, position 241,405,528. The table records no clinical significance for this variant.

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Reference-table entries

GPC1Not classified
Variant type
missense_variant
Chromosome / position
2:241405528
HGVS
NM_002081.3,c.1498A>G,p.Ser500Gly
Allele change
Missense_S500G

Public references

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