Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.38 (A)
Location

Chromosome 2:127257108 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs57011903, rs52816401

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 5 transcripts, has 2859 sample genotypes and is mentioned in 1 citation.

Variant displays