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:49070766 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.49070766C>T

About this variant

This variant overlaps 28 transcripts and has 1 individual genotype.

Variation displays