Original source

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

Alleles
T/A | Ancestral: A | Ambiguity code: W | MAF: 0.03 (A)
Location

Chromosome 3:58413147 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

3:g.58413147T>A

Variation displays