Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.09 (C)
Location

Chromosome X:49071510 (forward strand)|View in location tab

Most severe consequence
 
3 prime UTR variant
Evidence status

HGVS names

This variant has 3 HGVS names - Show

About this variant

This variant overlaps 44 transcripts and has 2505 sample genotypes.

Variant displays