Original source

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

HGVS names

This variant has 4 HGVS names - Show

About this variant

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

Variant displays