Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.01 (A)
Location

Chromosome 4:154604563 (forward strand)|View in location tab

Most severe consequence
 
Non coding transcript exon variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, has 2614 sample genotypes and is mentioned in 1 citation.

Variant displays