Original source

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

Alleles
-/AAT/ATA | MAF: 0.23 (-)
Location

Chromosome 6: between 144037703 and 144037704 (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 rs140506447

This variation has 24 HGVS names - click the plus to show

About this variant

This variant overlaps 22 transcripts and has 2510 individual genotypes.

Variation displays