Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.02 (A)

Chromosome 6:118548340 (forward strand) | View in location tab

Most severe consequence
5 prime UTR variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 8 transcripts, 1 regulatory feature, has 3272 sample genotypes and is associated with 1 phenotype.

Variant displays