Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.08 (G)
Location

Chromosome 3:122257406 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Clinical significance

This variant has 3 synonyms - click the plus to show

This variant has 4 HGVS names - click the plus to show

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 2656 sample genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays