Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.47 (T)
Location

Chromosome 19:10154572 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 8 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 8 transcripts, has 2777 sample genotypes and is mentioned in 4 citations.

Variant displays