Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.19 (C)
Location

Chromosome X:49070766 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

X:g.49070766C>T

About this variant

This variant overlaps 39 transcripts and has 2505 sample genotypes.

Variant displays