Original source

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

C/G|Ancestral: T|Ambiguity code: S|MAF: < 0.01 (G)

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

Most severe consequence
Non coding transcript exon variant
Evidence status


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

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 2 transcripts and has 2504 sample genotypes.

Variant displays