Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.04 (A)
Location

Chromosome 18:5392293 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

18:g.5392293G>A

About this variant

This variant overlaps 12 transcripts and has 2505 sample genotypes.

Variant displays