Variant (rsID / SNP)

rs148402761

rs148402761 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to DRD5. Location: chromosome 4, position 9,783,915. Clinical significance in the table: Benign.

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Reference-table entries

DRD5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 4:9783915
Cytoband: 4p16.1
HGVS: NM_000798.5(DRD5):c.262C>T (p.Leu88Phe)
Allele change: Missense_L88F

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.