Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.20 (A)
Location

Chromosome 17:17237369 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

This variant has 2 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 9 transcripts, 1 regulatory feature, has 3871 sample genotypes and is mentioned in 1 citation.

Variant displays