Original source

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

Alleles
-/G | MAF: 0.17 (G)
Location

Chromosome 12: between 21131691 and 21131692 (forward strand) | View in location tab

Most severe consequence

This variation has 6 HGVS names - click the plus to show

Variation displays