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, HumanCoreExome-12

About this variant

This variant overlaps 6 transcripts, is associated with 2 phenotypes and is mentioned in 2 citations.

Variation displays