Variant (rsID / SNP)

rs3749966

rs3749966 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TSBP1. Location: chromosome 6, position 32,261,507. The table records no clinical significance for this variant.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

TSBP1Not classified

Variant type: missense_variant
Chromosome / position: 6:32261507
HGVS: NM_006781.5,c.943A>G,p.Ile315Val
Allele change: Silent

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.