Variant (rsID / SNP)

rs146147877

rs146147877 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC27A5. Location: chromosome 19, position 59,023,213. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SLC27A5Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 19:59023213
Cytoband: 19q13.43
HGVS: NM_012254.3(SLC27A5):c.110T>G (p.Leu37Arg)
Allele change: Missense_L37R

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.