Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 2:204732223 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

2:g.204732223T>A

Genotyping chips

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

Variation displays