Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.37 (C)

Chromosome X:48901927 (forward strand) | View in location tab

Most severe consequence
Splice region variant
Evidence status


Archive dbSNP rs3817682

HGVS names

This variant has 17 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 35 transcripts, has 3810 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays