Original source

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

G/T | Ancestral: G | Ambiguity code: K | MAF: 0.08 (T)

Chromosome X:37783152 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs34853679

HGVS names

This variant has 5 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts and has 2550 sample genotypes.

Variant displays