Original source

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

Alleles
T/A/G | Ancestral: T | Ambiguity code: D | MAF: 0.03 (A)
Location

Chromosome 6:15523652 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 20 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 30 transcripts and has 2506 individual genotypes.

Variation displays