Variant (rsID / SNP)

rs13928

rs13928 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AEBP1. Location: chromosome 7, position 44,153,780. The table records no clinical significance for this variant.

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Reference-table entries

AEBP1Not classified

Variant type: missense_variant
Chromosome / position: 7:44153780
HGVS: NM_001129.5,c.3397A>G,p.Lys1133Glu
Allele change: Missense_K1133E

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.