Original source

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

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