Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | 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
Evidence status

Clinical significance

Synonyms

LSDB 6969, 2010_April_001_370_ZIC3_300265_0004

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

Variation displays