Original source

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

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

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

Most severe consequence
Evidence status


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

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 46 transcripts and has 1227 individual genotypes.

Variation displays