This variant has been flagged

Variation has more than 3 different alleles

Original source

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

Alleles
C/A/G/T | Ancestral: C | Ambiguity code: N
Location

Chromosome X:49923007 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs56981136, rs17174087

This variant has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature and has 4 sample genotypes.

Variant displays