Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: < 0.01 (A)
Location

Chromosome X:46911744 (forward strand) | View in location tab

Most severe consequence
HGVS name

X:g.46911744T>A

Variation displays