Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome X:154535277 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM880030

Most severe consequence
Evidence status

Clinical significance

This variation has 5 synonyms - click the plus to show

This variation has 19 HGVS names - click the plus to show

Genotyping chips

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

About this variant

This variant overlaps 13 transcripts, has 66 individual genotypes, is associated with 3 phenotypes and is mentioned in 16 citations.

Variation displays