Variant (rsID / SNP)

rs893184

rs893184 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to A1BG. Location: chromosome 19, position 58,864,479. The table records no clinical significance for this variant.

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Reference-table entries

A1BGNot classified

Variant type: missense_variant
Chromosome / position: 19:58864479
HGVS: NM_130786.4,c.155A>G,p.His52Arg
Allele change: Missense_H52R

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.