Original source

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

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

Chromosome X:154531643 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3174484

This variation has 4 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, HumanCoreExome-12, Illumina_HumanOmni5

About this variant

This variant overlaps 12 transcripts, has 2 individual genotypes and is mentioned in 3 citations.

Variation displays