Original source

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

Alleles
G/-|Ancestral: G|MAF: 0.39 (G)
Location

Chromosome 11:47349934 (forward strand)|View in location tab

Co-located variant

dbSNP rs181840234 (G/A)

Most severe consequence
 
Intron variant
Evidence status

Clinical significance

Synonyms
HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 7 transcripts, has 2593 sample genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays