Original source

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

Alleles
G/A/T | Ancestral: G | Ambiguity code: D | MAF: 0.27 (A)
Location

Chromosome 8:22164421 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 10 HGVS names - click the plus to show

Variation displays