Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.06 (T)
Location

Chromosome 20:46709087 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

20:g.46709087C>T

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 2 transcripts, 1 regulatory feature, has 3688 sample genotypes and is mentioned in 1 citation.

Variant displays