Original source

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

A/C/G | Ancestral: A | Ambiguity code: V | MAF: 0.37 (G)

Chromosome 5:136048754 (forward strand) | View in location tab

Most severe consequence
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 16 HGVS names - Show

About this variant

This variant overlaps 18 transcripts and has 2601 sample genotypes.

Variant displays