Original source

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

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

Chromosome X:154153068 (forward strand) | View in location tab

Co-located

with COSMIC COSM3759420 (T/G), COSM3759419 (T/G) ; HGMD-PUBLIC CM045803

Most severe consequence
Evidence status

Clinical significance

This variation has 7 synonyms - click the plus to show

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

Genotyping chips

This variation has assays on: Illumina_ExomeChip

About this variant

This variant overlaps 3 transcripts, has 35 individual genotypes and is associated with 2 phenotypes.

Variation displays