Variant (rsID / SNP)

rs149709084

rs149709084 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SLC27A5. Location: chromosome 19, position 59,012,027. Clinical significance in the table: Likely benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

SLC27A5Likely benign

Clinical significance (as recorded): Likely benign
Variant type: single nucleotide variant
Chromosome / position: 19:59012027
Cytoband: 19q13.43
HGVS: NM_012254.3(SLC27A5):c.1229G>A (p.Gly410Glu)
Allele change: Missense_G326E

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.