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:136046675 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and 2 regulatory features.

Variant displays