Variant (rsID / SNP)

rs34642241

rs34642241 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to LYST. Location: chromosome 1, position 235,909,815. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

LYSTBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 1:235909815
Cytoband: 1q42.3
HGVS: NM_000081.4(LYST):c.7793T>A (p.Phe2598Tyr)
Allele change: Missense_F2598Y

Associated conditions / phenotypes

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.