Original source

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

C/T | Ancestral: C | Ambiguity code: Y

Chromosome X:154776309 (forward strand) | View in location tab


with COSMIC COSM3759429 (C/T)

Most severe consequence
Synonymous variant
Evidence status

Clinical significance


This variant has 6 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 15 transcripts, has 1105 sample genotypes and is associated with 1 phenotype.

Variant displays