Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [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
Evidence status

Synonyms
HGVS name

2:g.203867500T>A

Genotyping chips

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

Variation displays