Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.17 (A)
Location

Chromosome 11:72059556 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 18 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Affy GeneChip 500K, Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1

Variation displays