Original source

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

Alleles
G/C|Ancestral: G|Ambiguity code: S|MAF: 0.25 (G)
Location

Chromosome X:46460623 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs2104468, rs5905543

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2506 sample genotypes.

Variant displays