Variant (rsID / SNP)

rs1042719

rs1042719 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADRB2. Location: chromosome 5, position 148,207,447. The table records no clinical significance for this variant.

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Reference-table entries

ADRB2Not classified

Variant type: synonymous_variant
Chromosome / position: 5:148207447
HGVS: NM_000024.6,c.1053G>C,p.Gly351Gly
Allele change: Synonymous_G351G

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.