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:48523786 (forward strand) | View in location tab

Co-located

with COSMIC COSM150788 (G/T)

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

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 17 transcripts, has 1227 individual genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variation displays