Variant (rsID / SNP)

rs180753337

rs180753337 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLCE1. Location: chromosome 10, position 96,014,770. Clinical significance in the table: Uncertain significance.

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Reference-table entries

PLCE1Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 10:96014770
Cytoband: 10q23.33
HGVS: NM_016341.4(PLCE1):c.3518C>T (p.Ser1173Phe)
Allele change: Missense_S1173F

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.