Original source

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

G/A/T | Ancestral: G | Ambiguity code: D | MAF: 0.05 (T)

Chromosome 15:64162924 (forward strand) | View in location tab

Most severe consequence
Synonymous variant
Evidence status

Clinical significance

HGVS names

This variant has 16 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 12 transcripts, 1 regulatory feature, has 3472 sample genotypes and is associated with 1 phenotype.

Variant displays