Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.04 (A)
Location

Chromosome X:31478314 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM940360 ; PhenCode DMD:c.8729A>G (T/C), DMD:c.8729A>T (T/A)

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 26 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12, Illumina_HumanOmni5

Variation displays