This variant has been flagged

Variation has more than 3 different alleles

Original source

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

C/A/G/T | Ancestral: C | Ambiguity code: N | MAF: < 0.01 (T)

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17174087, rs56981136

HGVS names

This variant has 9 HGVS names - Show

About this variant

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

Variant displays