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:3615831 (forward strand) | View in location tab

Co-located

with COSMIC COSM108888 (G/A)

Most severe consequence
Evidence status

Clinical significance

Synonyms

LSDB NC_000023.9:g.3543872G>A

This variation has 4 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip, HumanCoreExome-12

Somatic mutation displays