Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.20 (T)
Location

Chromosome 3:58427942 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3181868, rs1126698

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_ImmunoChip, Illumina_HumanOmni5

About this variant

This variant overlaps 20 transcripts and has 2507 individual genotypes.

Variation displays