Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S
Location

Chromosome X:50003843 (forward strand) | View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs56766896

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

About this variant

This variant overlaps 7 transcripts and has 273 sample genotypes.

Variant displays