Variant (rsID / SNP)

rs267606783

rs267606783 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ENG. Location: chromosome 9, position 130,616,633. Clinical significance in the table: Pathogenic.

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Reference-table entries

ENGPathogenic

Clinical significance (as recorded): Pathogenic
Variant type: single nucleotide variant
Chromosome / position: 9:130616633
Cytoband: 9q34.11
HGVS: NM_001114753.3(ENG):c.2T>C (p.Met1Thr)
Allele change: Missense_M1T

Associated conditions / phenotypes

Telangiectasia, hereditary hemorrhagic, type 1

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.