Variant (rsID / SNP)

rs28932173

rs28932173 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLCL2. Location: chromosome 3, position 17,051,450. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PLCL2Not classified

Variant type: synonymous_variant
Chromosome / position: 3:17051450
HGVS: NM_001144382.2,c.612C>A,p.Arg204Arg
Allele change: Missense_Q201K

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.