Variant (rsID / SNP)

rs12139100

rs12139100 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLA2G2C. Location: chromosome 1, position 20,501,582. The table records no clinical significance for this variant.

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Reference-table entries

PLA2G2CNot classified

Variant type: stop_gained
Chromosome / position: 1:20501582
HGVS: NM_001316722.3,c.97C>T,p.Arg33*
Allele change: Nonsense_R33X

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.