Original source

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

Alleles
G/A/C|Ancestral: G|Ambiguity code: V|MAF: 0.14 (A)
Location

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

Most severe consequence
 
3 prime UTR variant
Evidence status

Clinical significance

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 32 transcripts, has 3682 sample genotypes and is associated with 1 phenotype.

Variant displays