Original source

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

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

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs111197527, rs60220920

HGVS names

This variant has 14 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 15 transcripts and has 3879 sample genotypes.

Variant displays