Original source

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

Alleles
-/AAT/ATA
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 10 HGVS names - click the plus to show

Variation displays