Variant (rsID / SNP)

rs4994

rs4994 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADRB3. Location: chromosome 8, position 37,823,798. Clinical significance in the table: Benign.

ShareE-Mail WhatsApp LinkedIn X Facebook Telegram

Reference-table entries

ADRB3Benign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 8:37823798
Cytoband: 8p11.23
HGVS: NM_000025.3(ADRB3):c.190T>C (p.Trp64Arg)
Allele change: Missense_W64R

Associated conditions / phenotypes

Obesity

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.