Original source

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

G/T | Ancestral: T | Ambiguity code: K | MAF: 0.38 (G)

Chromosome X:43731789 (forward strand) | View in location tab


with COSMIC COSM4156846 (G/T) ; HGMD-PUBLIC CM073190

Most severe consequence
Synonymous variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 3 transcripts, has 3802 sample genotypes, is associated with 1 phenotype and is mentioned in 23 citations.

Variant displays