Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome X:3522144 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.3522144C>A

Variation displays