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: 0.18 (T)
Location

Chromosome 20:766241 (forward strand) | View in location tab

Most severe consequence

 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]

Evidence status

Synonyms

Archive dbSNP rs57849739

This variation has 4 HGVS names - click the plus to show

Variation displays