Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.36 (A)
Location

Chromosome 11:47331947 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs3729803, rs56656921

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 17 transcripts, has 3682 sample genotypes and is associated with 1 phenotype.

Variant displays