Variant (rsID / SNP)

rs863223816

rs863223816 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TGFBR1. Location: chromosome 9, position 101,904,832. Clinical significance in the table: Likely pathogenic.

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Reference-table entries

TGFBR1Likely pathogenic

Clinical significance (as recorded): Likely pathogenic
Variant type: single nucleotide variant
Chromosome / position: 9:101904832
Cytoband: 9q22.33
HGVS: NM_004612.4(TGFBR1):c.820A>G (p.Thr274Ala)
Allele change: Missense_T197A

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.