Variant (rsID / SNP)

rs17885228

rs17885228 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SFTPD. Location: chromosome 10, position 81,702,538. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SFTPDBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 10:81702538
Cytoband: 10q22.3
HGVS: NM_003019.5(SFTPD):c.297G>A (p.Lys99=)
Allele change: Synonymous_K99K

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.