Original source

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

Alleles
A/C/G|Ancestral: G|Ambiguity code: V|MAF: 0.30 (G)
Location

Chromosome X:19355721 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Clinical significance

HGVS names

This variant has 22 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 32 transcripts, has 3589 sample genotypes and is associated with 2 phenotypes.

Variant displays