Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.04 (C)
Location

Chromosome X:31478309 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM940361 ; PhenCode DMD:c.8734A>G (T/C)

Most severe consequence
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

This variation has 24 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays