Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.47 (G)
Location

Chromosome 1:155299985 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs57506287, rs386578630

HGVS names

This variant has 4 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_ImmunoChip, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 3 transcripts, has 2859 sample genotypes and is mentioned in 1 citation.

Variant displays