Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.10 (T)

Chromosome 12:110913382 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

Clinical significance

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 4 transcripts, 1 regulatory feature, has 2772 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays