Original source

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

Alleles
-/TA | MAF: 0.23 (-)
Location

Chromosome 6: between 144037702 and 144037703 (forward strand) | View in location tab

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

This variation has 5 HGVS names - click the plus to show

Variation displays