Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.02 (A)
Location

Chromosome 3:15496343 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 8 HGVS names - click the plus to show

Variation displays