Original source

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

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

Chromosome X:18924184 (forward strand) | View in location tab

Most severe consequence
 
Non coding transcript exon variant
| See all predicted consequences [Genes and regulation]
Evidence status

Synonyms

LSDB NM_000292.2:c.1715-50G>C

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 2 transcripts.

Variation displays