Variant (rsID / SNP)

rs1050152

rs1050152 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC22A4. Location: chromosome 5, position 131,676,320. Clinical significance in the table: Benign.

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Reference-table entries

SLC22A4Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:131676320
Cytoband: 5q31.1
HGVS: NM_003059.3(SLC22A4):c.1507C>T (p.Leu503Phe)
Allele change: Missense_L503F

Associated conditions / phenotypes

SLC22A4 POLYMORPHISM

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.