Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
T/A | Ancestral: A | Ambiguity code: W | MAF: 0.30 (T)
Location

Chromosome 5:147203906 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58423060

HGVS name

5:g.147203906T>A

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0

Variation displays