Original source

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

Alleles
-/AAA | MAF: 0.01 (AAA)
Location

Chromosome 14: between 28765233 and 28765234 (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 rs373724317

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

About this variant

This variant overlaps 5 transcripts and has 2505 individual genotypes.

Variation displays