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:32438372 (forward strand) | View in location tab

Co-located

with COSMIC COSM1467596 (G/A), COSM1467595 (G/A), COSM1467594 (G/A) ; HGMD-PUBLIC CS002446, CM100263 ; PhenCode DMD:c.3940C>T (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB 7192

This variation has 15 HGVS names - click the plus to show

Variation displays