Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome X:38367350 (forward strand) | View in location tab

Co-located

with COSMIC COSM3766934 (A/C), COSM3759494 (A/G)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 5 HGVS names - click the plus to show

This variation has assays on 13 chips - click the plus to show

About this variant

This variant overlaps 3 transcripts, has 1634 individual genotypes, is associated with 2 phenotypes and is mentioned in 2 citations.

Variation displays