Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.25 (A)
Location

Chromosome X:19359975 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3181928

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2506 sample genotypes.

Variant displays