Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/A/T | Ancestral: G | Ambiguity code: D | MAF: < 0.01 (A)

Chromosome 9:22003719 (forward strand) | View in location tab

Most severe consequence
3 prime UTR variant
Evidence status

HGVS names

This variant has 36 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 38 transcripts and has 2504 sample genotypes.

Variant displays