Original source

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

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

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

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms
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