Original source

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

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

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