Original source

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

Alleles
C/A | Ancestral: G | Ambiguity code: M | MAF: 0.16 (A)
Location

Chromosome 17:7080758 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs59997287

HGVS name

17:g.7080758C>A

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 6 transcripts and has 3889 sample genotypes.

Variant displays