Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.03 (T)
Location

Chromosome 20:50891355 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17788801, rs58565808

This variation has 6 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays