Original source

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

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

Chromosome X:134458472 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

X:g.134458472A>C

About this variant

This variant overlaps 2 transcripts.

Variant displays