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:29941729 (forward strand) | View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Uniprot VAR_062263

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

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 2 transcripts and 1 regulatory feature.

Variant displays