Original source

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

Alleles
C/T|Ancestral: T|Ambiguity code: Y|MAF: 0.02 (T)
Location

Chromosome X:142206020 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs386561919

HGVS name

X:g.142206020C>T

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 1 transcript and has 3271 sample genotypes.

Variant displays