Variant (rsID / SNP)

rs72552709

rs72552709 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ALB. Location: chromosome 4, position 74,270,112. Clinical significance in the table: other.

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Reference-table entries

ALBOther

Clinical significance (as recorded): other
Variant type: single nucleotide variant
Chromosome / position: 4:74270112
Cytoband: 4q13.3
HGVS: NM_000477.7(ALB):c.68G>A (p.Arg23His)
Allele change: Missense_R23H

Associated conditions / phenotypes

PROALBUMIN LILLE

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.