Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

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

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3181928

This variant has 5 HGVS names - click the plus to show

About this variant

This variant overlaps 12 transcripts and has 2 sample genotypes.

Variant displays