Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.20 (C)
Location

Chromosome 12:111791045 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 5 HGVS names - click the plus to show

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, has 3684 sample genotypes and is mentioned in 2 citations.

Variant displays