Original source

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

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.48 (A)
Location

Chromosome X:48529077 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

Synonyms

Archive dbSNP rs57410751

HGVS name

X:g.48529077A>C

Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 7 transcripts and has 3690 sample genotypes.

Variant displays