Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.44 (T)
Location

Chromosome X:154051703 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs61565722

HGVS names

This variant has 14 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 16 transcripts, 1 regulatory feature, has 3739 sample genotypes and is mentioned in 2 citations.

Variant displays