Original source

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

Synonyms
HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

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

About this variant

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

Variant displays