Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.33 (T)
Location

Chromosome 3:50254761 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58074030

This variation has 11 HGVS names - click the plus to show

This variation has assays on 9 chips - click the plus to show

Variation displays