Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.05 (C)
Location

Chromosome 11:72015122 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_031680

This variation has 14 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, Illumina_HumanOmni5, Illumina_1M-duo

Variation displays