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Variant (rsID / SNP)

rs3749117

PLA2R1

rs3749117 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLA2R1. Location: chromosome 2, position 160,885,442. The table records no clinical significance for this variant.

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Reference-table entries

PLA2R1Not classified
Variant type
missense_variant
Chromosome / position
2:160885442
HGVS
NM_007366.5,c.874A>G,p.Met292Val
Allele change
Missense_M292V

Associated conditions / phenotypes

Membranous Nephropathy|Autoimmune Disease|Nephrotic Syndrome

Public references

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