Variant (rsID / SNP)

rs4905204

rs4905204 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SERPINA9. Location: chromosome 14, position 94,936,107. The table records no clinical significance for this variant.

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Reference-table entries

SERPINA9Not classified

Variant type: missense_variant
Chromosome / position: 14:94936107
HGVS: NM_175739.4,c.71C>T,p.Ala24Val
Allele change: Missense_A42V

Associated conditions / phenotypes

Atherosclerosis Susceptibility

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.