Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W|MAF: 0.25 (T)
Location

Chromosome 13:27919352 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 2 transcripts and has 2509 sample genotypes.

Variant displays