Variant (rsID / SNP)

rs138750527

rs138750527 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PER2. Location: chromosome 2, position 239,160,264. Clinical significance in the table: Likely benign.

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Reference-table entries

PER2Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 2:239160264
Cytoband: 2q37.3
HGVS: NM_022817.3(PER2):c.3250T>C (p.Cys1084Arg)
Allele change: Missense_C1084R

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.