Original source

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

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

Chromosome X:137564567 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.137564567T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 6 transcripts.

Variation displays