Original source

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

T/A | Ancestral: T | Ambiguity code: W | MAF: 0.39 (A)

Chromosome X:120456678 (forward strand) | View in location tab


with COSMIC COSM4156559 (T/A), COSM4156558 (T/A), COSM4156557 (T/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Affy GenomeWideSNP_6.0, Illumina_HumanOmni5

About this variant

This variant overlaps 7 transcripts, has 2585 individual genotypes and is associated with 2 phenotypes.

Variation displays