This variation has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
C/A/G/T | Ancestral: C | Ambiguity code: N
Location

Chromosome X:154770804 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM990479

Most severe consequence
Evidence status

Clinical significance

This variation has 2 synonyms - click the plus to show

This variation has 42 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_ImmunoChip, Illumina_HumanOmni5

About this variant

This variant overlaps 48 transcripts, has 549 individual genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variation displays