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:48825698 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.48825698T>C

About this variant

This variant overlaps 9 transcripts.

Variation displays