Variant (rsID / SNP)

rs41302657

rs41302657 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ENG. Location: chromosome 9, position 130,581,016. Clinical significance in the table: Benign/Likely benign.

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Reference-table entries

ENGBenign

Clinical significance (as recorded): Benign/Likely benign
Variant type: single nucleotide variant
Chromosome / position: 9:130581016
Cytoband: 9q34.11
HGVS: NM_001114753.3(ENG):c.1407G>A (p.Pro469_Gly470=)
Allele change: Synonymous_P469P

Associated conditions / phenotypes

Telangiectasia, hereditary hemorrhagic, type 1|Hereditary hemorrhagic telangiectasia

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.