Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W
Location

Chromosome X:49070875 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
HGVS name

X:g.49070875T>A

About this variant

This variant overlaps 29 transcripts.

Variant displays