Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.22 (G)
Location

Chromosome 3:58427791 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1801428, rs3181916

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

This variation has assays on 6 chips - click the plus to show

Variation displays