Variant (rsID / SNP)

rs142821701

rs142821701 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GPD2. Location: chromosome 2, position 157,369,961. Clinical significance in the table: Uncertain significance.

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Reference-table entries

GPD2Uncertain significance

Clinical significance (as recorded): Uncertain significance
Variant type: single nucleotide variant
Chromosome / position: 2:157369961
Cytoband: 2q24.1
HGVS: NM_000408.5(GPD2):c.614C>T (p.Pro205Leu)
Allele change: Missense_P205L

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.