Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP
Chromosome X:18941678 (forward strand) | View in location tab
This variation has 2 synonyms - click the plus to show
This variation has 2 HGVS names - click the plus to show
This variation has assays on: Illumina_HumanOmni5
This variant overlaps 1 transcript.