Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.36 (A)
Location

Chromosome 2:208124313 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 3 synonyms - click the plus to show

This variation has 2 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 3 transcripts, has 3722 individual genotypes and is mentioned in 2 citations.

Variation displays