Variant (rsID / SNP)

rs1135062

rs1135062 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to BCAM. Location: chromosome 19, position 45,322,744. 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: 19:45322744
Cytoband: 19q13.32
HGVS: NM_005581.5(BCAM):c.1615A>G (p.Thr539Ala)
Allele change: Missense_T539A

Associated conditions / phenotypes

AUBERGER BLOOD GROUP POLYMORPHISM Au(a)/Au(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.