Original source

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

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

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

Most severe consequence
3 prime UTR variant
Evidence status


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