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Variant (rsID / SNP)

rs753381

PLCG1

rs753381 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLCG1. Location: chromosome 20, position 39,797,465. The table records no clinical significance for this variant.

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Reference-table entries

PLCG1Not classified
Variant type
missense_variant
Chromosome / position
20:39797465
HGVS
NM_002660.3,c.2438T>C,p.Ile813Thr
Allele change
Missense_I813T

Associated conditions / phenotypes

Urticaria|Angioedema

Public references

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