Original source

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

G/T | Ancestral: T | Ambiguity code: K

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


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

Most severe consequence
Evidence status

Clinical significance


This variation has 3 HGVS names - click the plus to show

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 1298 individual genotypes and is mentioned in 22 citations.

Variation displays