Original source

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

Alleles
AT/- | MAF: 0.11 (-)
Location

Chromosome 2:231514173-231514174 (forward strand) | View in location tab

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

Synonyms

This variation has 2 HGVS names - click the plus to show

Variation displays