Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/A/G|Ancestral: C|Ambiguity code: V
Location

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

Co-located variant

HGMD-PUBLIC CM990479

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS names

This variant has 28 HGVS names - Show

Genotyping chips

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

About this variant

This variant overlaps 32 transcripts, has 549 sample genotypes, is associated with 2 phenotypes and is mentioned in 1 citation.

Variant displays