Variant (rsID / SNP)

rs145948919

rs145948919 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PIEZO2. Location: chromosome 18, position 10,979,655. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PIEZO2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 18:10979655
Cytoband: 18p11.21
HGVS: NM_001378183.1(PIEZO2):c.164A>C (p.His55Pro)
Allele change: Missense_H55P

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.