Variant (rsID / SNP)

rs56392308

rs56392308 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ABO. Location: chromosome 9, position 136,131,057. Clinical significance in the table: Affects.

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Reference-table entries

ABOOther

Clinical significance (as recorded): Affects
Variant type: Deletion
Chromosome / position: 9:136131057
Cytoband: 9q34.2
HGVS: NM_020469.3(ABO):c.1061del (p.Pro354fs)

Associated conditions / phenotypes

ABO blood group system

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.