Original source

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

Alleles
A/C/T | Ancestral: A | Ambiguity code: H
Location

Chromosome X:38367353 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CD982840, CM062942, CM971094

Most severe consequence
Evidence status

Clinical significance

This variation has 3 synonyms - click the plus to show

This variation has 10 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ExomeChip

Variation displays