Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: < 0.01 (G)
Location

Chromosome X:133592263 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

X:g.133592263A>G

Variation displays