Original source

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

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

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59725696, rs57568245

This variation has 5 HGVS names - click the plus to show

Genotyping chips

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

About this variant

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

Variation displays