Original source

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

C/T | Ambiguity code: Y

Chromosome X:154037187 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs6643811

HGVS names

This variant has 18 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 19 transcripts and has 1070 sample genotypes.

Variant displays