Original source

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

Alleles
T/C | Ambiguity code: Y
Location

Chromosome X:46911408 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs6521168, rs57397176

HGVS name

X:g.46911408T>C

About this variant

This variant overlaps 4 transcripts and has 1 sample genotype.

Variant displays