Original source

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

Alleles
G/A/T | Ancestral: A | Ambiguity code: D | MAF: 0.36 (G)
Location

Chromosome 14:73163562 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 44 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays