Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome X:48688723 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM072118

Most severe consequence
 
Missense variant
Evidence status

This variant has 7 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 8 transcripts and is mentioned in 1 citation.

Variant displays