This variant has been flagged

Variation has more than 3 different alleles

Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/C/G/T | Ancestral: A | Ambiguity code: N | MAF: < 0.01 (G)
Location

Chromosome 11:5225488 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR045224, CR014260, CR850010 ; PhenCode HbVar.968 (A/G)

Most severe consequence
 
3 prime UTR variant
Evidence status

Clinical significance

This variant has 4 synonyms - click the plus to show

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts, 1 regulatory feature, has 2504 sample genotypes, is associated with 2 phenotypes and is mentioned in 6 citations.

Variant displays