Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/G | Ancestral: A | Ambiguity code: R
Location

Chromosome X:136651213 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM040508

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 6971, 2010_April_001_372_ZIC3_300265_0006

This variation has 6 HGVS names - click the plus to show

Variation displays