Variant (rsID / SNP)

rs121909569

rs121909569 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SERPINC1. Location: chromosome 1, position 173,881,119. Clinical significance in the table: Pathogenic.

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Reference-table entries

SERPINC1Pathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 1:173881119
Cytoband: 1q25.1
HGVS: NM_000488.4(SERPINC1):c.442T>C (p.Ser148Pro)
Allele change: Missense_S148P

Associated conditions / phenotypes

Hereditary antithrombin deficiency

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.