Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/T|Ancestral: A|Ambiguity code: W|MAF: 0.27 (T)
Location

Chromosome 1:7982342 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs406533, rs1173409, rs835732

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

Variant displays