Variant (rsID / SNP)

rs334353

rs334353 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TGFBR1. Location: chromosome 9, position 101,908,365. The table records no clinical significance for this variant.

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Reference-table entries

TGFBR1Not classified

Variant type: single nucleotide variant
Chromosome / position: 9:101908365
Cytoband: 9q22.33
HGVS: NM_004612.4(TGFBR1):c.1131-402T>G
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.