Original source

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

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

Chromosome X:154644304 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs2294121, rs370731140

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 1 transcript.

Variant displays