Original source

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

Alleles
A/- | Ancestral: A | MAF: 0.49 (A)
Location

Chromosome 11:18400461 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

This variation has 21 HGVS names - click the plus to show

Variation displays