Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.30 (G)
Location

Chromosome 5:136047539 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

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

About this variant

This variant overlaps 9 transcripts and has 2532 sample genotypes.

Variant displays