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
G/A/C/T | Ancestral: G | Ambiguity code: N
Location

Chromosome X:154776873 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Clinical significance

This variant has 18 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 48 transcripts, has 1178 sample genotypes and is associated with 1 phenotype.

Variant displays