Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.03 (T)
Location

Chromosome 19:10116025 (forward strand) | View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

This variant has 7 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 27 transcripts, has 3124 sample genotypes and is associated with 1 phenotype.

Variant displays