Variant (rsID / SNP)

rs11546882

rs11546882 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to POC1A. Location: chromosome 3, position 52,183,958. Clinical significance in the table: Benign.

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Reference-table entries

POC1ABenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 3:52183958
Cytoband: 3p21.2
HGVS: NM_015426.5(POC1A):c.149C>T (p.Pro50Leu)
Allele change: Missense_P50L

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.