Original source

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

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

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