Variant (rsID / SNP)

rs10511687

rs10511687 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FOCAD. Location: chromosome 9, position 20,764,870. Clinical significance in the table: Benign.

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Reference-table entries

FOCADBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 9:20764870
Cytoband: 9p21.3
HGVS: NM_001375567.1(FOCAD):c.497T>C (p.Leu166Ser)
Allele change: Missense_L166S

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.