Variant (rsID / SNP)

rs137853867

rs137853867 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PPIB. Location: chromosome 15, position 64,452,302. Clinical significance in the table: Pathogenic.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

PPIBPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 15:64452302
Cytoband: 15q22.31
HGVS: NM_000942.5(PPIB):c.343+1G>A
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.