Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.09 (T)
Location

Chromosome X:48827185 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

X:g.48827185C>T

About this variant

This variant overlaps 10 transcripts and has 2505 sample genotypes.

Variant displays