Variant (rsID / SNP)

rs28399653

rs28399653 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BCAM. Location: chromosome 19, position 45,315,445. Clinical significance in the table: Benign.

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Reference-table entries

BCAMBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:45315445
Cytoband: 19q13.32
HGVS: NM_005581.4(BCAM):c.230G>A (p.Arg77His)
Allele change: Missense_R77H

Associated conditions / phenotypes

LUTHERAN BLOOD GROUP POLYMORPHISM Lu(a)/Lu(b)

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.