Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome X:133304844 (forward strand) | View in location tab

Co-located

with COSMIC COSM3736490 (C/A)

Most severe consequence
Evidence status

This variation has 4 synonyms - click the plus to show

This variation has 3 HGVS names - click the plus to show

This variation has assays on 10 chips - click the plus to show

About this variant

This variant overlaps 1 transcript and has 1223 individual genotypes.

Variation displays