Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.10 (A)

Chromosome X:154536951 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs59845413, rs17336780

HGVS names

This variant has 12 HGVS names - Show

Genotyping chips

This variant has assays on: Affy GenomeWideSNP_6.0, Illumina_CytoSNP12v1, Illumina_HumanOmni5

About this variant

This variant overlaps 14 transcripts, has 4017 sample genotypes and is mentioned in 2 citations.

Variant displays