Variant (rsID / SNP)

rs6113

rs6113 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SERPINA5. Location: chromosome 14, position 95,053,849. The table records no clinical significance for this variant.

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Reference-table entries

SERPINA5Not classified

Variant type: synonymous_variant
Chromosome / position: 14:95053849
HGVS: NM_000624.6,c.150T>C,p.Phe50Phe
Allele change: Synonymous_F50F

Associated conditions / phenotypes

Obsessive-Compulsive Disorder

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.