Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome X:152855469 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17327009

This variant has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 72 sample genotypes.

Variant displays