Original source

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

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.22 (G)
Location

Chromosome 6:6143728 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

6:g.6143728T>G

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 1 transcript and has 2510 sample genotypes.

Variant displays