Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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
 
Synonymous variant
Evidence status

Synonyms

This variant has 3 synonyms - Show

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

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

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature, has 3722 sample genotypes and is mentioned in 2 citations.

Variant displays