Original source

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

Alleles
T/A | Ancestral: A | Ambiguity code: W | MAF: 0.32 (T)
Location

Chromosome 12:40315611 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 5 HGVS names - click the plus to show

Genotyping chips

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

About this variant

This variant overlaps 4 transcripts, has 4139 individual genotypes and is mentioned in 1 citation.

Variation displays