Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.06 (T)

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


with COSMIC COSM3759429 (C/T)

Most severe consequence
Evidence status

Clinical significance


This variation has 6 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 15 transcripts, has 2198 individual genotypes and is associated with 1 phenotype.

Variation displays