Original source

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

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

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

Co-located variant

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