Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs386561919

HGVS name

X:g.142206020C>T

This variation has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 1 transcript and has 767 individual genotypes.

Variation displays