Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K
Location

Chromosome X:120427048 (forward strand) | View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

Synonyms

Archive dbSNP rs3174394

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

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature and has 2 sample genotypes.

Variant displays