Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.41 (G)
Location

Chromosome 12:132648860 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

Synonyms

Archive dbSNP rs57182744

This variant has 7 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 2602 sample genotypes.

Variant displays