Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.10 (G)
Location

Chromosome 22:29285227 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs111197527, rs60220920

This variant has 14 HGVS names - click the plus to 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 15 transcripts and has 3879 sample genotypes.

Variant displays