Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S
Location

Chromosome X:19350562 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 11 transcripts.

Variant displays