Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/G | Ancestral: G | Ambiguity code: K | MAF: 0.05 (T)
Location

Chromosome 11:46097373 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 12 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 11 transcripts and has 2559 sample genotypes.

Variant displays