Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.20 (G)
Location

Chromosome 17:4898299 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

This variant has 3 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 17 transcripts, has 2509 sample genotypes and is mentioned in 1 citation.

Variant displays