Variant (rsID / SNP)

rs1804495

rs1804495 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SERPINA7. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SERPINA7Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Cytoband: Xq22.3
HGVS: NM_000354.5(SERPINA7):c.909G>T (p.Leu303Phe)
Allele change: Missense_L303F

Associated conditions / phenotypes

Thyroxine-binding globulin, variant P|Thyroxine-binding globulin quantitative trait locus

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.