Variant (rsID / SNP)

rs1805017

rs1805017 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLA2G7. Location: chromosome 6, position 46,684,222. The table records no clinical significance for this variant.

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Reference-table entries

PLA2G7Not classified

Variant type: single nucleotide variant
Chromosome / position: 6:46684222
Cytoband: 6p12.3
HGVS: NM_005084.4(PLA2G7):c.275G>A (p.Arg92His)
Allele change: Missense_R92H

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.