Variant (rsID / SNP)

rs3729604

rs3729604 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ADRA1B. Location: chromosome 5, position 159,344,461. The table records no clinical significance for this variant.

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Reference-table entries

ADRA1BNot classified

Variant type: synonymous_variant
Chromosome / position: 5:159344461
HGVS: NM_000679.4,c.549G>A,p.Gly183Gly
Allele change: Synonymous_G183G

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.