Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.29 (T)
Location

Chromosome X:120426744 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs58259470, rs3174393

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 5 transcripts and has 3080 sample genotypes.

Variant displays