Original source

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

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

Chromosome X:154181480 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs147319455

HGVS name

X:g.154181480G>A

About this variant

This variant overlaps 2 transcripts and has 1 sample genotype.

Variant displays