Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.41 (G)
Location

Chromosome 8:93924304 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

This variant has 4 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

About this variant

This variant overlaps 10 transcripts, has 2515 sample genotypes and is mentioned in 1 citation.

Variant displays