Variant (rsID / SNP)

rs1042713

rs1042713 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADRB2. Location: chromosome 5, position 148,206,440. Clinical significance in the table: Benign.

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Reference-table entries

ADRB2Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 5:148206440
Cytoband: 5q32
HGVS: NM_000024.6(ADRB2):c.46= (p.Gly16=)
Allele change: Missense_G16R

Associated conditions / phenotypes

Asthma, nocturnal, susceptibility to

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.