Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.01 (T)
Location

Chromosome 12:52681126 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

12:g.52681126T>C

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K

About this variant

This variant overlaps 2 transcripts and has 3719 sample genotypes.

Variant displays