Original source

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

Alleles
T/G | Ambiguity code: K | MAF: 0.49 (T)
Location

Chromosome 20:5307854 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57093393

This variation has 2 HGVS names - click the plus to show

Variation displays