Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.23 (T)
Location

Chromosome 6:98832781 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

6:g.98832781C>T

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 1 transcript and has 2507 sample genotypes.

Variant displays