Variant (rsID / SNP)

rs182937977

rs182937977 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PLG. Location: chromosome 6, position 161,155,096. Clinical significance in the table: Uncertain significance.

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Reference-table entries

PLGUncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 6:161155096
Cytoband: 6q26
HGVS: NM_000301.5(PLG):c.1657G>A (p.Asp553Asn)
Allele change: Missense_D553N

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.