Original source

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

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

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

Co-located variant

HGMD-PUBLIC CM040506

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 6969, 2010_April_001_370_ZIC3_300265_0004

HGVS names

This variant has 5 HGVS names - Show

About this variant

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

Variant displays