Original source

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

Most severe consequence
Evidence status

This variation has 19 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 18 transcripts and has 2511 individual genotypes.

Variation displays