Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome 11:72004078 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Uniprot VAR_051248

This variation has 17 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni5, Illumina_Human1M-duo

Variation displays