Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

T/C/G | Ancestral: C | Ambiguity code: B | MAF: 0.01 (T)

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

Most severe consequence
Upstream gene variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

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

About this variant

This variant overlaps 4 transcripts and has 3719 sample genotypes.

Variant displays