Original source

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

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

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

Most severe consequence
 
Splice region variant
Evidence status

Synonyms

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 43 transcripts, has 3810 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays