Original source

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

Alleles
T/A | Ancestral: A | Ambiguity code: W | MAF: 0.04 (T)
Location

Chromosome 2:203867500 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms
HGVS name

2:g.203867500T>A

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Affy GeneChip 500K, Illumina_ImmunoChip

About this variant

This variant overlaps 5 transcripts, has 3622 sample genotypes and is mentioned in 1 citation.

Variant displays