Original source

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

Alleles
-/GAG/TGA | MAF: 0.42 (-)
Location

Chromosome 16: between 89096237 and 89096238 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 18 HGVS names - click the plus to show

Variation displays