Variant (rsID / SNP)

rs148153072

rs148153072 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLCL2. Location: chromosome 3, position 16,926,766. The table records no clinical significance for this variant.

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Reference-table entries

PLCL2Not classified

Variant type: synonymous_variant
Chromosome / position: 3:16926766
HGVS: NM_001144382.2,c.228C>T,p.Pro76Pro
Allele change: Missense_P73S

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.