Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

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

Chromosome X:31206663 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM980563 ; PhenCode DMD:c.9568C>T (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_081_DMD_300377_0076, 7191

This variation has 34 HGVS names - click the plus to show

Variation displays