Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.21 (A)
Location

Chromosome 12:56041628 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

This variant has 2 HGVS names - click the plus to show

This variant has assays on 7 chips - click the plus to show

About this variant

This variant overlaps 8 transcripts, 1 regulatory feature, has 3690 sample genotypes and is mentioned in 3 citations.

Variant displays