Original source

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

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

Chromosome 12:21852233 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

Clinical significance


This variant has 2 synonyms - Show

HGVS names

This variant has 16 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 12 transcripts, 1 regulatory feature, has 2506 sample genotypes and is associated with 2 phenotypes.

Variant displays