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:120426744 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs58259470, rs3174393

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

About this variant

This variant overlaps 5 transcripts and has 576 sample genotypes.

Variant displays