Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.28 (C)
Location

Chromosome 11:47350826 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 7 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip

About this variant

This variant overlaps 9 transcripts, has 2539 individual genotypes and is associated with 1 phenotype.

Variation displays