Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.19 (G)
Location

Chromosome 6:6143711 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

6:g.6143711A>G

This variant has assays on 6 chips - click the plus to show

About this variant

This variant overlaps 1 transcript and has 2509 sample genotypes.

Variant displays