Variant (rsID / SNP)

rs284878

rs284878 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TGFBR3. Location: chromosome 1, position 92,174,260. The table records no clinical significance for this variant.

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Reference-table entries

TGFBR3Not classified

Variant type: synonymous_variant
Chromosome / position: 1:92174260
HGVS: NM_003243.5,c.2247T>C,p.Thr749Thr
Allele change: Synonymous_T748T

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.