Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
-/TTG | MAF: 0.03 (TTG)
Location

Chromosome 2: between 9629285 and 9629286 (forward strand) | View in location tab

Most severe consequence

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

Variation displays