Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.06 (T)
Location

Chromosome X:154776309 (forward strand)|View in location tab

Most severe consequence
 
Synonymous variant
Evidence status

Synonyms

This variant has 5 synonyms - Show

HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 15 transcripts, has 3609 sample genotypes and is associated with 1 phenotype.

Variant displays