Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/A/T | Ancestral: C | Ambiguity code: H

Chromosome X:2955804 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 10 HGVS names - Show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 12 transcripts and has 1239 sample genotypes.

Variant displays