Variant (rsID / SNP)

rs55646160

rs55646160 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIEZO2. Location: chromosome 18, position 10,794,753. Clinical significance in the table: Benign.

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Reference-table entries

PIEZO2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 18:10794753
Cytoband: 18p11.22
HGVS: NM_001378183.1(PIEZO2):c.1758+17C>T
Allele change: Silent

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.