Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/A/T | Ancestral: G | Ambiguity code: D | MAF: 0.24 (A)

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

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 52 transcripts, 1 regulatory feature, has 2508 sample genotypes and is mentioned in 1 citation.

Variant displays