Variant (rsID / SNP)

rs2070862

rs2070862 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SERPINF2. Location: chromosome 17, position 1,648,294. Clinical significance in the table: Benign.

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Reference-table entries

SERPINF2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 17:1648294
Cytoband: 17p13.3
HGVS: NM_000934.4(SERPINF2):c.5C>T (p.Ala2Val)
Allele change: Missense_A2V

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.