Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome X:137567436 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM040506

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 6969, 2010_April_001_370_ZIC3_300265_0004

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and is associated with 2 phenotypes.

Variant displays