Original source

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

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

Chromosome X:2959835 (forward strand) | View in location tab

Most severe consequence
 
5 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs59531228

This variant has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 3 sample genotypes.

Variant displays