Original source

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

A/G | Ambiguity code: R | MAF: 0.40 (G)

Chromosome 20:54156357 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59725696, rs57568245

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Affy GenomeWideSNP_6.0, Affy GeneChip 500K

About this variant

This variant overlaps 4 transcripts, has 3961 sample genotypes and is mentioned in 2 citations.

Variant displays