Original source

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

G/C | Ancestral: G | Ambiguity code: S | MAF: < 0.01 (C)

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

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs56766896

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2777 sample genotypes.

Variant displays