Original source

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

Alleles
G/C/T | Ancestral: G | Ambiguity code: B
Location

Chromosome 17:42200049 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant

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

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 6 transcripts.

Variant displays