Variant (rsID / SNP)

rs1045916

rs1045916 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BAIAP2L1, BRI3. Location: chromosome 7, position 97,933,601. The table records no clinical significance for this variant.

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Reference-table entries

BAIAP2L1Not classified

Variant type: synonymous_variant
Chromosome / position: 7:97933601
HGVS: NM_018842.5,c.1329G>A,p.Leu443Leu
Allele change: Synonymous_L443L

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.