Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.43 (G)

Chromosome 6:143946046 (forward strand) | View in location tab


with dbSNP rs68014771 (G/A/GG/-)

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs28627035, rs11414469

This variant has 17 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 19 transcripts and has 2509 sample genotypes.

Variant displays