Variant (rsID / SNP)

rs1880736

rs1880736 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABCA13. Location: chromosome 7, position 48,315,796. The table records no clinical significance for this variant.

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Reference-table entries

ABCA13Not classified

Variant type: missense_variant
Chromosome / position: 7:48315796
HGVS: NM_152701.5,c.6533C>A,p.Ala2178Glu
Allele change: Missense_A2178E

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.