Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y
Location

Chromosome X:19342596 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.19342596C>T

Genotyping chips

This variation has assays on: Illumina_Human1M-duo, Affy GenomeWideSNP_6.0, Illumina_HumanOmni5

About this variant

This variant overlaps 9 transcripts and has 835 individual genotypes.

Variation displays