Original source

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

C/A/G|Ancestral: C|Ambiguity code: V

Chromosome X:154765450 (forward strand)|View in location tab

Co-located variants

HGMD-PUBLIC CM042697, CM058293

Most severe consequence
Missense variant
Evidence status

Clinical significance


LSDB NM_001363.3:c.91C>G, NM_001363.3:c.91C>A, 6830

HGVS names

This variant has 30 HGVS names - Show

About this variant

This variant overlaps 28 transcripts and is associated with 3 phenotypes.

Variant displays