Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V | MAF: < 0.01 (C)
Location

Chromosome X:32519950 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM930192 ; PhenCode DMD:c.2302C>T (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 26261

This variation has 22 HGVS names - click the plus to show

Variation displays