Original source

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

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 9 transcripts and has 2868 sample genotypes.

Variant displays