Variant (rsID / SNP)

rs1131364

rs1131364 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to FETUB. Location: chromosome 3, position 186,370,333. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

FETUBNot classified

Variant type: synonymous_variant
Chromosome / position: 3:186370333
HGVS: NM_001375587.2,c.1062G>T,p.Val354Val
Allele change: Synonymous_V289V

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.