Variant (rsID / SNP)

rs74370122

rs74370122 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ASAP1. Location: chromosome 8, position 131,165,000. The table records no clinical significance for this variant.

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Reference-table entries

ASAP1Not classified

Variant type: synonymous_variant
Chromosome / position: 8:131165000
HGVS: NM_001362924.1,c.1071G>A,p.Leu357Leu
Allele change: Synonymous_L354L

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.