Original source

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

Alleles
AC/- | MAF: 0.04 (-)
Location

Chromosome 16:2634821-2634822 (forward strand) | View in location tab

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

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

Variation displays