Original source

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

Alleles
C/A|Ancestral: A|Ambiguity code: M|MAF: 0.04 (A)
Location

Chromosome X:3604103 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

X:g.3604103C>A

About this variant

This variant overlaps 3 transcripts and has 2504 sample genotypes.

Variant displays