Variant (rsID / SNP)

rs10838677

rs10838677 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ACP2. Location: chromosome 11, position 47,267,079. Clinical significance in the table: Benign.

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Reference-table entries

ACP2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 11:47267079
Cytoband: 11p11.2
HGVS: NM_001610.4(ACP2):c.495G>A (p.Leu165=)
Allele change: Synonymous_L137L

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.