Variant (rsID / SNP)

rs1320191

rs1320191 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TLN2. Location: chromosome 15, position 63,009,804. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TLN2Not classified

Variant type: synonymous_variant
Chromosome / position: 15:63009804
HGVS: NM_001394547.1,c.2793C>T,p.Ala931Ala
Allele change: Synonymous_A931A

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.