Original source

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

C/G | Ancestral: G | Ambiguity code: S | MAF: 0.22 (C)

Chromosome 6:143974397 (forward strand) | View in location tab


with dbSNP rs767266167 (C/-)

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 19 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 18 transcripts and has 2691 sample genotypes.

Variant displays