Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

Chromosome X:19355513 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 15 transcripts.

Variant displays