Original source

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

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

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

Most severe consequence
Evidence status


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

About this variant

This variant overlaps 53 transcripts, has 1103 individual genotypes and is mentioned in 1 citation.

Variation displays