Variant (rsID / SNP)

rs151043891

rs151043891 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to AFF2. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

AFF2Benign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Cytoband: Xq28
HGVS: NM_002025.4(AFF2):c.2656C>G (p.Pro886Ala)
Allele change: Missense_P851A

Associated conditions / phenotypes

Intellectual disability

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.