Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.05 (T)
Location

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

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

Synonyms

This variant has 6 HGVS names - click the plus to show

Genotyping chips

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

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 3472 sample genotypes and is associated with 1 phenotype.

Variant displays