Original source

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

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

Chromosome X:31196901 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM084898, CS921169 ; PhenCode DMD:c.10108C>T (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 7122, 2010_April_001_071_DMD_300377_0007

This variation has 31 HGVS names - click the plus to show

Variation displays