Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
C/T | Ambiguity code: Y
Location

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

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs6643811

This variation has 18 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Illumina_HumanOmni5

About this variant

This variant overlaps 19 transcripts and has 1070 individual genotypes.

Variation displays