Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
-/ACAC | MAF: 0.40 (-)
Location

Chromosome 16: between 50741030 and 50741031 (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 rs140662501

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 14 transcripts and has 2504 individual genotypes.

Variation displays