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:154536313 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

This variant has 12 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 14 transcripts, has 855 sample genotypes and is mentioned in 2 citations.

Variant displays